TEST-DiseaseOrPhenotypicFeature  

PubMed:15041272 / 0-135 JSONTXT 7 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function

Id Subject Object Predicate Lexical cue #label
T1 36-66 DiseaseOrPhenotypicFeature denotes type 2B von Willebrand disease D056728
T2 114-128 DiseaseOrPhenotypicFeature denotes genetic defect DISEASE