release normalization step (#7363)

Author: sabrinatoro

src/ontology/mondo-edit.obo

@@ -2974,7 +2974,7 @@ is_a: MONDO:0005093 {source="DOID:0050204", source="MONDO:Redundant"} ! skin dis
 is_a: MONDO:0006011 {source="DOID:0050204", source="MONDO:Redundant"} ! viral hepatitis
 intersection_of: MONDO:0000001 ! disease
 intersection_of: disease_has_inflammation_site UBERON:0002107 ! liver
-intersection_of: MONDO:0100332 NCBITaxon:10376 ! disease has primary infectious agent Human gammaherpesvirus 4
+intersection_of: MONDO:0100332 NCBITaxon:10376 ! disease has primary infectious agent human gammaherpesvirus 4
 
 [Term]
 id: MONDO:0000287
@@ -14595,7 +14595,7 @@ xref: SCTID:4598005 {source="MONDO:equivalentTo", source="DOID:10573"}
 xref: UMLS:C0029442 {source="MONDO:notFoundInDiseaseSubset", source="DOID:10573", source="NCIT:C26838"}
 is_a: MONDO:0000833 {source="DOID:10573"} ! bone remodeling disease
 is_a: MONDO:0800486 {source="NCIT:C26838"} ! metabolic bone disorder
-relationship: disease_has_feature HP:0100512 ! Low levels of vitamin D
+relationship: disease_has_feature HP:0100512 ! Decreased circulating vitamin D concentration
 property_value: IAO:0000233 "https://github.com/monarch-initiative/mondo/issues/7006" xsd:anyURI
 property_value: IAO:0000589 "osteomalacia (disease)" xsd:string
 
@@ -34003,7 +34003,7 @@ xref: ICD9:373.31 {source="DOID:1893", source="MONDO:equivalentTo", source="MOND
 xref: SCTID:36259009 {source="DOID:1893", source="MONDO:equivalentTo"}
 xref: UMLS:C0155177 {source="DOID:1893", source="MONDO:equivalentTo"}
 is_a: MONDO:0002137 {source="DOID:1893"} ! noninfectious dermatoses of eyelid
-relationship: disease_has_feature HP:0000964 ! Eczema
+relationship: disease_has_feature HP:0000964 ! Eczematoid dermatitis
 
 [Term]
 id: MONDO:0002137
@@ -84081,9 +84081,9 @@ subset: inferred_rare
 subset: rare
 synonym: "granuloma, plasma cell, orbital" EXACT [MESH:D016727]
 synonym: "inflammatory pseudotumor of orbit" EXACT [MESH:D016727, UMLS:C0085270]
+synonym: "inflammatory pseudotumor of orbit proper" EXACT [SCTID:72789009]
 synonym: "inflammatory pseudotumor, orbital" EXACT [MESH:D016727]
 synonym: "inflammatory pseudotumors, orbital" EXACT [MESH:D016727]
-synonym: "inflammatory pseudotumor of orbit proper" EXACT [SCTID:72789009]
 synonym: "orbital granuloma, plasma cell" EXACT [MESH:D016727]
 synonym: "orbital inflammatory pseudotumor" EXACT [MESH:D016727]
 synonym: "orbital inflammatory pseudotumors" EXACT [MESH:D016727]
@@ -88079,7 +88079,7 @@ is_a: MONDO:0002406 {source="DOID:3310", source="EFO:0000274", source="MONDO:Red
 is_a: MONDO:0005271 {source="EFO:0000274", source="MONDO:Redundant"} ! allergic disease
 intersection_of: MONDO:0002406 ! dermatitis
 intersection_of: disease_has_basis_in_disruption_of GO:0016068 ! type I hypersensitivity
-relationship: disease_has_feature HP:0000964 ! Eczema
+relationship: disease_has_feature HP:0000964 ! Eczematoid dermatitis
 relationship: has_characteristic MONDO:0021152 {source="OMIMPS:603165"} ! inherited
 
 [Term]
@@ -92098,7 +92098,7 @@ xref: NCIT:C38759 {source="MONDO:equivalentTo", source="EFO:0000769"}
 xref: UMLS:C0149678 {source="MONDO:equivalentTo", source="NCIT:C38759"}
 is_a: MONDO:0005108 {source="EFO:0000769", source="MESH:D020031/inferred", source="MONDO:Redundant", source="NCIT:C38759"} ! viral infectious disease
 intersection_of: MONDO:0005550 ! infectious disease
-intersection_of: MONDO:0100332 NCBITaxon:10376 ! disease has primary infectious agent Human gammaherpesvirus 4
+intersection_of: MONDO:0100332 NCBITaxon:10376 ! disease has primary infectious agent human gammaherpesvirus 4
 
 [Term]
 id: MONDO:0005112
@@ -100903,7 +100903,7 @@ xref: SCTID:68295002 {source="MONDO:relatedTo", source="DOID:10609"}
 xref: UMLS:C0035579 {source="MONDO:equivalentTo", source="DOID:10609", source="NCIT:C26878"}
 xref: UMLS:C0221468 {source="MONDO:relatedTo", source="DOID:10609"}
 is_a: MONDO:0000833 {source="DOID:10609", source="PMID:20936937"} ! bone remodeling disease
-relationship: disease_has_feature HP:0100512 ! Low levels of vitamin D
+relationship: disease_has_feature HP:0100512 ! Decreased circulating vitamin D concentration
 property_value: IAO:0000589 "rickets (disease)" xsd:string
 
 [Term]
@@ -103402,7 +103402,7 @@ xref: SCTID:62251004 {source="MONDO:equivalentTo", source="DOID:2934"}
 xref: UMLS:C0002016 {source="MONDO:equivalentTo", source="DOID:2934"}
 is_a: MONDO:0005108 {source="DOID:2934", source="EFO:0007139", source="MESH:D000453/inferred"} ! viral infectious disease
 intersection_of: MONDO:0005550 ! infectious disease
-intersection_of: MONDO:0100332 NCBITaxon:28314 ! disease has primary infectious agent Aleutian mink disease virus
+intersection_of: MONDO:0100332 NCBITaxon:28314 ! disease has primary infectious agent Aleutian mink disease parvovirus
 
 [Term]
 id: MONDO:0005642
@@ -105355,7 +105355,7 @@ is_a: MONDO:0005135 {source="Orphanet:1546"} ! parasitic infectious disease
 intersection_of: MONDO:0005550 ! infectious disease
 intersection_of: disease_has_infectious_agent NCBITaxon:5207 ! Cryptococcus neoformans
 relationship: disease_has_infectious_agent NCBITaxon:5207 {source="MONDO:Wikidata"} ! Cryptococcus neoformans
-relationship: disease_has_infectious_agent NCBITaxon:552467 {source="MONDO:Wikidata"} ! Cryptococcus gattii VGIII
+relationship: disease_has_infectious_agent NCBITaxon:552467 {source="MONDO:Wikidata"} ! Cryptococcus bacillisporus
 relationship: has_characteristic MONDO:0021136 {source="MONDO:0015577"} ! rare
 relationship: has_characteristic MONDO:0045035 {source="https://www.ncbi.nlm.nih.gov/books/NBK7902/"} ! opportunistic infectious
 property_value: seeAlso "https://rarediseases.info.nih.gov/diseases/6218/cryptococcosis" xsd:anyURI {source="GARD:0006218"}
@@ -107264,7 +107264,7 @@ xref: UMLS:C0021345 {source="NCIT:C34726", source="DOID:8568", source="MONDO:equ
 is_a: MONDO:0005111 {source="MESH:D007244", source="MONDO:Redundant", source="NCIT:C34726"} ! Epstein-Barr virus infection
 relationship: disease_has_feature HP:0001744 ! Splenomegaly
 relationship: disease_has_feature HP:0002716 ! Lymphadenopathy
-relationship: disease_has_infectious_agent NCBITaxon:10376 {source="MONDO:Wikidata"} ! Human gammaherpesvirus 4
+relationship: disease_has_infectious_agent NCBITaxon:10376 {source="MONDO:Wikidata"} ! human gammaherpesvirus 4
 
 [Term]
 id: MONDO:0005811
@@ -108924,7 +108924,7 @@ xref: UMLS:C0027983 {source="DOID:2929", source="NCIT:C34849", source="MONDO:equ
 is_a: MONDO:0005108 {source="DOID:2929", source="EFO:0007395", source="MESH:D009521/inferred", source="NCIT:C34849"} ! viral infectious disease
 relationship: disease_has_feature HP:0000509 ! Conjunctivitis
 relationship: disease_has_feature HP:0003470 ! Paralysis
-relationship: disease_has_infectious_agent NCBITaxon:2560319 ! Avian orthoavulavirus 1
+relationship: disease_has_infectious_agent NCBITaxon:2560319 ! avian paramyxovirus 1
 
 [Term]
 id: MONDO:0005876
@@ -172696,7 +172696,7 @@ xref: SCTID:128596003 {source="MONDO:equivalentTo"}
 xref: UMLS:C0220710 {source="Orphanet:42", source="OMIM:201450", source="NCIT:C84538", source="MONDO:equivalentTo", source="MONDO:ncbi_mim2gene_medline", source="Orphanet:42/e"}
 is_a: MONDO:0017714 {source="Orphanet:42"} ! acyl-CoA dehydrogenase deficiency
 intersection_of: MONDO:0003847 ! hereditary disease
-intersection_of: disease_has_basis_in_disruption_of GO:0070991 ! medium-chain-acyl-CoA dehydrogenase activity
+intersection_of: disease_has_basis_in_disruption_of GO:0070991 ! medium-chain fatty acyl-CoA dehydrogenase activity
 relationship: has_material_basis_in_germline_mutation_in http://identifiers.org/hgnc/89 {source="MONDO:mim2gene_medgen"} ! ACADM
 property_value: confidence "3.2857142857142847" xsd:double
 property_value: IAO:0000233 "https://github.com/monarch-initiative/mondo/issues/4521" xsd:anyURI
@@ -172739,7 +172739,7 @@ xref: Orphanet:26792 {source="OMIM:201470", source="MONDO:equivalentTo"}
 xref: UMLS:C0342783 {source="OMIM:201470", source="NCIT:C84539", source="MONDO:ncbi_mim2gene_medline", source="MONDO:notFoundInDiseaseSubset"}
 is_a: MONDO:0017714 {source="Orphanet:26792"} ! acyl-CoA dehydrogenase deficiency
 intersection_of: MONDO:0003847 ! hereditary disease
-intersection_of: disease_has_basis_in_disruption_of GO:0016937 ! short-chain-acyl-CoA dehydrogenase activity
+intersection_of: disease_has_basis_in_disruption_of GO:0016937 ! short-chain fatty acyl-CoA dehydrogenase activity
 relationship: has_material_basis_in_germline_mutation_in http://identifiers.org/hgnc/90 {source="MONDO:mim2gene_medgen"} ! ACADS
 property_value: seeAlso "https://rarediseases.info.nih.gov/diseases/4822/short-chain-acyl-coa-dehydrogenase-deficiency" xsd:anyURI {source="GARD:0004822"}
 
@@ -172777,7 +172777,7 @@ is_a: MONDO:0005045 ! hypertrophic cardiomyopathy
 is_a: MONDO:0005267 ! heart disorder
 is_a: MONDO:0017713 ! disorder of fatty acid oxidation and ketogenesis
 intersection_of: MONDO:0003847 ! hereditary disease
-intersection_of: disease_has_basis_in_disruption_of GO:0017099 ! very-long-chain-acyl-CoA dehydrogenase activity
+intersection_of: disease_has_basis_in_disruption_of GO:0017099 ! very-long-chain fatty acyl-CoA dehydrogenase activity
 relationship: has_material_basis_in_germline_mutation_in http://identifiers.org/hgnc/92 {source="MONDO:mim2gene_medgen"} ! ACADVL
 property_value: confidence "0.20000000000000018" xsd:double
 
@@ -203334,7 +203334,7 @@ is_a: MONDO:0000424 {source="DOID:0050734", source="MESH:C563242/inferred", sour
 is_a: MONDO:0016624 ! inherited deficiency anemia
 is_a: MONDO:0019220 {source="Orphanet:332"} ! inborn disorder of cobalamin metabolism and transport
 relationship: disease_has_feature HP:0001889 ! Megaloblastic anemia
-relationship: disease_has_feature HP:0100502 ! Vitamin B12 deficiency
+relationship: disease_has_feature HP:0100502 ! Decreased circulating vitamin B12 concentration
 relationship: has_material_basis_in_germline_mutation_in http://identifiers.org/hgnc/4268 {source="MONDO:mim2gene_medgen"} ! CBLIF
 property_value: confidence "2.2500000000000004" xsd:double
 
@@ -440421,7 +440421,7 @@ is_a: MONDO:0005045 ! hypertrophic cardiomyopathy
 is_a: MONDO:0005267 ! heart disorder
 is_a: MONDO:0017713 ! disorder of fatty acid oxidation and ketogenesis
 intersection_of: MONDO:0019052 ! inborn errors of metabolism
-intersection_of: disease_has_basis_in_disruption_of GO:0004466 ! long-chain-acyl-CoA dehydrogenase activity
+intersection_of: disease_has_basis_in_disruption_of GO:0004466 ! long-chain fatty acyl-CoA dehydrogenase activity
 
 [Term]
 id: MONDO:0020532
@@ -443231,7 +443231,7 @@ xref: UMLS:C0042847 {source="MONDO:equivalentTo", source="NCIT:C131684"}
 is_a: MONDO:0042976 {source="NCIT:C131684"} ! vitamin B deficiency
 intersection_of: MONDO:0005066 ! metabolic disease
 intersection_of: disease_has_basis_in_disruption_of GO:0009235 ! cobalamin metabolic process
-relationship: disease_has_feature HP:0100502 ! Vitamin B12 deficiency
+relationship: disease_has_feature HP:0100502 ! Decreased circulating vitamin B12 concentration
 
 [Term]
 id: MONDO:0020697
@@ -530582,9 +530582,9 @@ def: "Triploidy that occurs in tench." [MONDO:patterns/nonhuman_disease]
 xref: OMIA:001180-27717 {source="MONDO:equivalentTo"}
 is_a: MONDO:1010031 {source="OMIA:001180", source="https://orcid.org/0000-0002-5002-8648"} ! triploidy, non-human animal
 intersection_of: MONDO:0005583 ! non-human animal disease
-intersection_of: in_taxon NCBITaxon:27717
+intersection_of: in_taxon NCBITaxon:27717 ! Tinca tinca
 intersection_of: MONDO:0700097 MONDO:0018067 ! cross-species analog triploidy
-relationship: in_taxon NCBITaxon:27717 {source="OMIA:001180-27717", source="https://orcid.org/0000-0002-5002-8648"}
+relationship: in_taxon NCBITaxon:27717 {source="OMIA:001180-27717", source="https://orcid.org/0000-0002-5002-8648"} ! Tinca tinca
 property_value: IAO:0000233 "https://github.com/monarch-initiative/mondo/issues/7075" xsd:anyURI
 
 [Term]
@@ -530706,9 +530706,9 @@ def: "Cleft palate that occurs in spectacled flying fox." [MONDO:patterns/nonhum
 xref: OMIA:000197-328804 {source="MONDO:equivalentTo"}
 is_a: MONDO:1010037 {source="OMIA:000197", source="https://orcid.org/0000-0002-5002-8648"} ! cleft palate, non-human animal
 intersection_of: MONDO:0005583 ! non-human animal disease
-intersection_of: in_taxon NCBITaxon:328804
+intersection_of: in_taxon NCBITaxon:328804 ! Pteropus conspicillatus
 intersection_of: MONDO:0700097 MONDO:0016064 ! cross-species analog cleft palate
-relationship: in_taxon NCBITaxon:328804 {source="OMIA:000197-328804", source="https://orcid.org/0000-0002-5002-8648"}
+relationship: in_taxon NCBITaxon:328804 {source="OMIA:000197-328804", source="https://orcid.org/0000-0002-5002-8648"} ! Pteropus conspicillatus
 property_value: IAO:0000233 "https://github.com/monarch-initiative/mondo/issues/7075" xsd:anyURI
 
 [Term]
@@ -532493,9 +532493,9 @@ def: "AA amyloidosis that occurs in island gray fox." [MONDO:patterns/nonhuman_d
 xref: OMIA:000038-244585 {source="MONDO:equivalentTo"}
 is_a: MONDO:1010092 {source="OMIA:000038", source="https://orcid.org/0000-0002-5002-8648"} ! AA amyloidosis, non-human animal
 intersection_of: MONDO:0005583 ! non-human animal disease
-intersection_of: in_taxon NCBITaxon:244585
+intersection_of: in_taxon NCBITaxon:244585 ! Urocyon littoralis
 intersection_of: MONDO:0700097 MONDO:0019439 ! cross-species analog AA amyloidosis
-relationship: in_taxon NCBITaxon:244585 {source="OMIA:000038-244585", source="https://orcid.org/0000-0002-5002-8648"}
+relationship: in_taxon NCBITaxon:244585 {source="OMIA:000038-244585", source="https://orcid.org/0000-0002-5002-8648"} ! Urocyon littoralis
 property_value: IAO:0000233 "https://github.com/monarch-initiative/mondo/issues/7075" xsd:anyURI
 
 [Term]
@@ -532749,10 +532749,10 @@ def: "Galactosemia that occurs in kangaroo." [MONDO:patterns/nonhuman_disease]
 xref: OMIA:001144-9322 {source="MONDO:equivalentTo"}
 is_a: MONDO:1010101 {source="OMIA:001144", source="https://orcid.org/0000-0002-5002-8648"} ! galactosemia, non-human animal
 intersection_of: MONDO:0005583 ! non-human animal disease
-intersection_of: in_taxon NCBITaxon:9322
+intersection_of: in_taxon NCBITaxon:9322 ! Macropus sp.
 intersection_of: MONDO:0700097 MONDO:0018116 ! cross-species analog galactosemia
 relationship: excluded_from_qc_check http://purl.obolibrary.org/obo/mondo/sparql/qc/general/qc-single-child.sparql
-relationship: in_taxon NCBITaxon:9322 {source="OMIA:001144-9322", source="https://orcid.org/0000-0002-5002-8648"}
+relationship: in_taxon NCBITaxon:9322 {source="OMIA:001144-9322", source="https://orcid.org/0000-0002-5002-8648"} ! Macropus sp.
 property_value: IAO:0000233 "https://github.com/monarch-initiative/mondo/issues/7075" xsd:anyURI
 
 [Term]
@@ -533806,9 +533806,9 @@ def: "Syndactyly that occurs in Swainson's hawk." [MONDO:patterns/nonhuman_disea
 xref: OMIA:000963-156757 {source="MONDO:equivalentTo"}
 is_a: MONDO:1010160 {source="OMIA:000963", source="https://orcid.org/0000-0002-5002-8648"} ! syndactyly, non-human animal
 intersection_of: MONDO:0005583 ! non-human animal disease
-intersection_of: in_taxon NCBITaxon:156757
+intersection_of: in_taxon NCBITaxon:156757 ! Buteo swainsoni
 intersection_of: MONDO:0700097 MONDO:0021002 ! cross-species analog syndactyly
-relationship: in_taxon NCBITaxon:156757 {source="OMIA:000963-156757", source="https://orcid.org/0000-0002-5002-8648"}
+relationship: in_taxon NCBITaxon:156757 {source="OMIA:000963-156757", source="https://orcid.org/0000-0002-5002-8648"} ! Buteo swainsoni
 property_value: IAO:0000233 "https://github.com/monarch-initiative/mondo/issues/7075" xsd:anyURI
 
 [Term]
@@ -534112,9 +534112,9 @@ def: "Lysosomal storage disease that occurs in kangaroo." [MONDO:patterns/nonhum
 xref: OMIA:000616-9322 {source="MONDO:equivalentTo"}
 is_a: MONDO:1010171 {source="OMIA:000616", source="https://orcid.org/0000-0002-5002-8648"} ! lysosomal storage disease, non-human animal
 intersection_of: MONDO:0005583 ! non-human animal disease
-intersection_of: in_taxon NCBITaxon:9322
+intersection_of: in_taxon NCBITaxon:9322 ! Macropus sp.
 intersection_of: MONDO:0700097 MONDO:0002561 ! cross-species analog lysosomal storage disease
-relationship: in_taxon NCBITaxon:9322 {source="OMIA:000616-9322", source="https://orcid.org/0000-0002-5002-8648"}
+relationship: in_taxon NCBITaxon:9322 {source="OMIA:000616-9322", source="https://orcid.org/0000-0002-5002-8648"} ! Macropus sp.
 property_value: IAO:0000233 "https://github.com/monarch-initiative/mondo/issues/7075" xsd:anyURI
 
 [Term]
@@ -535033,9 +535033,9 @@ def: "Hydrocephalus that occurs in yellow-crowned parrot." [MONDO:patterns/nonhu
 xref: OMIA:000487-151761 {source="MONDO:equivalentTo"}
 is_a: MONDO:1010233 {source="OMIA:000487", source="https://orcid.org/0000-0002-5002-8648"} ! hydrocephalus, non-human animal
 intersection_of: MONDO:0005583 ! non-human animal disease
-intersection_of: in_taxon NCBITaxon:151761
+intersection_of: in_taxon NCBITaxon:151761 ! Amazona ochrocephala
 intersection_of: MONDO:0700097 MONDO:0001150 ! cross-species analog hydrocephalus
-relationship: in_taxon NCBITaxon:151761 {source="OMIA:000487-151761", source="https://orcid.org/0000-0002-5002-8648"}
+relationship: in_taxon NCBITaxon:151761 {source="OMIA:000487-151761", source="https://orcid.org/0000-0002-5002-8648"} ! Amazona ochrocephala
 property_value: IAO:0000233 "https://github.com/monarch-initiative/mondo/issues/7075" xsd:anyURI
 
 [Term]
@@ -535919,9 +535919,9 @@ def: "Urolithiasis that occurs in kangaroo." [MONDO:patterns/nonhuman_disease]
 xref: OMIA:001033-9322 {source="MONDO:equivalentTo"}
 is_a: MONDO:1010267 {source="OMIA:001033", source="https://orcid.org/0000-0002-5002-8648"} ! urolithiasis, non-human animal
 intersection_of: MONDO:0005583 ! non-human animal disease
-intersection_of: in_taxon NCBITaxon:9322
+intersection_of: in_taxon NCBITaxon:9322 ! Macropus sp.
 intersection_of: MONDO:0700097 MONDO:0024647 ! cross-species analog urolithiasis
-relationship: in_taxon NCBITaxon:9322 {source="OMIA:001033-9322", source="https://orcid.org/0000-0002-5002-8648"}
+relationship: in_taxon NCBITaxon:9322 {source="OMIA:001033-9322", source="https://orcid.org/0000-0002-5002-8648"} ! Macropus sp.
 property_value: IAO:0000233 "https://github.com/monarch-initiative/mondo/issues/7075" xsd:anyURI
 
 [Term]
@@ -537174,9 +537174,9 @@ def: "Synovial chondromatosis that occurs in great horned owl." [MONDO:patterns/
 xref: OMIA:001174-56268 {source="MONDO:equivalentTo"}
 is_a: MONDO:1010304 {source="OMIA:001174", source="https://orcid.org/0000-0002-5002-8648"} ! synovial chondromatosis, non-human animal
 intersection_of: MONDO:0005583 ! non-human animal disease
-intersection_of: in_taxon NCBITaxon:56268
+intersection_of: in_taxon NCBITaxon:56268 ! Bubo virginianus
 intersection_of: MONDO:0700097 MONDO:0006438 ! cross-species analog synovial chondromatosis
-relationship: in_taxon NCBITaxon:56268 {source="OMIA:001174-56268", source="https://orcid.org/0000-0002-5002-8648"}
+relationship: in_taxon NCBITaxon:56268 {source="OMIA:001174-56268", source="https://orcid.org/0000-0002-5002-8648"} ! Bubo virginianus
 property_value: IAO:0000233 "https://github.com/monarch-initiative/mondo/issues/7075" xsd:anyURI
 
 [Term]
@@ -537686,9 +537686,9 @@ def: "Microphthalmia that occurs in Eastern wapiti." [MONDO:patterns/nonhuman_di
 xref: OMIA:000649-9861 {source="MONDO:equivalentTo"}
 is_a: MONDO:1010324 {source="OMIA:000649", source="https://orcid.org/0000-0002-5002-8648"} ! microphthalmia, non-human animal
 intersection_of: MONDO:0005583 ! non-human animal disease
-intersection_of: in_taxon NCBITaxon:9861
+intersection_of: in_taxon NCBITaxon:9861 ! Cervus canadensis canadensis
 intersection_of: MONDO:0700097 MONDO:0021129 ! cross-species analog microphthalmia
-relationship: in_taxon NCBITaxon:9861 {source="OMIA:000649-9861", source="https://orcid.org/0000-0002-5002-8648"}
+relationship: in_taxon NCBITaxon:9861 {source="OMIA:000649-9861", source="https://orcid.org/0000-0002-5002-8648"} ! Cervus canadensis canadensis
 property_value: IAO:0000233 "https://github.com/monarch-initiative/mondo/issues/7075" xsd:anyURI
 
 [Term]