This is a preliminary release of the MedMentions dataset, a corpus of Biomedical papers annotated with mentions of UMLS entities. CZI Meta is releasing this data to promote NLP research on Biomedical text.
This data is being released under the CC0 license. The papers in the corpus were selected from those available from PubMed® / Medline®. Users are referred to that source for the most current and accurate version of the text for the corresponding papers.
Corpus: The MedMentions corpus consists of 4,392 papers (Titles and Abstracts) randomly selected from among papers released on PubMed in 2016, that were in the biomedical field, published in the English language, and had both a Title and an Abstract.
Annotators: We recruited a team of professional annotators with rich experience in biomedical content curation to exhaustively annotate all UMLS® (2017AA full version) entity mentions in these papers.
Annotation quality: We did not collect stringent IAA (Inter-annotator agreement) data. To gain insight on the annotation quality of MedMentions, we randomly selected eight papers from the annotated corpus, containing a total of 469 concepts. Two biologists ('Reviewer') who did not participate in the annotation task then each reviewed four papers. The agreement between Reviewers and Annotators, an estimate of the Precision of the annotations, was 97.3%.
- full: This is the full dataset
We will also publish some task-specific subsets of this data.
The annotated data is published in PubTator format:
Each paper or document ends with a blank line, and is represented as (without the spaces):
PMID | t | Title text
PMID | a | Abstract text
PMID TAB StartIndex TAB EndIndex TAB MentionTextSegment TAB SemanticTypeID TAB EntityID
...
The first two lines present the Title and Abstract texts (no line-breaks or tabs in the text). Subsequent lines present the mentions, one per line. The StartIndex and EndIndex are 0-based character indices into the document text, constructed by concatenating the Title and Abstract, separated by a SPACE character. The MentionTextSegment is the actual mention between those character positions. The EntityID is the UMLS entity (concept) id, and the SemanticTypeID is the id for the Semantic Type that entity is linked to in UMLS. If the UMLS entity is linked to more than one semantic type, then this field contains the lowest common ancestor. All UMLS concepts that are not in the 2017-AA Active release are linked to the special semantic type UnknownType.
Here is an example:
25763772|t|DCTN4 as a modifier of chronic Pseudomonas aeruginosa infection in cystic fibrosis
25763772|a|Pseudomonas aeruginosa (Pa) infection in cystic fibrosis (CF) patients is associated with worse long-term pulmonary disease and shorter survival, and chronic Pa infection (CPA) is associated with reduced lung function, faster rate of lung decline, increased rates of exacerbations and shorter survival. By using exome sequencing and extreme phenotype design, it was recently shown that isoforms of dynactin 4 (DCTN4) may influence Pa infection in CF, leading to worse respiratory disease. The purpose of this study was to investigate the role of DCTN4 missense variants on Pa infection incidence, age at first Pa infection and chronic Pa infection incidence in a cohort of adult CF patients from a single centre. Polymerase chain reaction and direct sequencing were used to screen DNA samples for DCTN4 variants. A total of 121 adult CF patients from the Cochin Hospital CF centre have been included, all of them carrying two CFTR defects: 103 developed at least 1 pulmonary infection with Pa, and 68 patients of them had CPA. DCTN4 variants were identified in 24% (29/121) CF patients with Pa infection and in only 17% (3/18) CF patients with no Pa infection. Of the patients with CPA, 29% (20/68) had DCTN4 missense variants vs 23% (8/35) in patients without CPA. Interestingly, p.Tyr263Cys tend to be more frequently observed in CF patients with CPA than in patients without CPA (4/68 vs 0/35), and DCTN4 missense variants tend to be more frequent in male CF patients with CPA bearing two class II mutations than in male CF patients without CPA bearing two class II mutations (P = 0.06). Our observations reinforce that DCTN4 missense variants, especially p.Tyr263Cys, may be involved in the pathogenesis of CPA in male CF.
25763772 0 5 DCTN4 T103 C4308010
25763772 23 63 chronic Pseudomonas aeruginosa infection T038 C0854135
25763772 67 82 cystic fibrosis T038 C0010674
25763772 83 120 Pseudomonas aeruginosa (Pa) infection T038 C0854135
...
In this example, the Title is 82 characters long. The first mention is for the UMLS concept "DCTN4 protein, human" whose UMLS id is C4308010. This entity is linked to two semantic types: "Amino Acid, Peptide, or Protein" (T116) and "Biologically Active Substance" (T123), whose lowest common ancestor is "Chemical" (T103 ).
A more formal release will be published soon. Until then, please cite the following paper:
Shikhar Murty, Patrick Verga, Luke Vilnis, Irena Radovanovic and Andrew McCallum. Hierarchical Losses and New Resources for Fine-grained Entity Typing and Linking. The 56th Annual Meeting of the Association for Computational Linguistics (ACL). Melbourne, Australia. July 2018.
If you have any comments, questions or issues, please post a note in GitHub issues.