PubMed:15041272 / 89-206
Annnotations
TEST-DiseaseOrPhenotypicFeature
| Id | Subject | Object | Predicate | Lexical cue | #label |
|---|---|---|---|---|---|
| T2 | 25-39 | DiseaseOrPhenotypicFeature | denotes | genetic defect | DISEASE |
| T3 | 67-97 | DiseaseOrPhenotypicFeature | denotes | type 2B von Willebrand disease | D056728 |
| T4 | 99-102 | DiseaseOrPhenotypicFeature | denotes | VWD | D014842 |
Test-merged-2
| Id | Subject | Object | Predicate | Lexical cue | #label |
|---|---|---|---|---|---|
| T2 | 25-39 | DiseaseOrPhenotypicFeature | denotes | genetic defect | DISEASE |
| T3 | 67-97 | DiseaseOrPhenotypicFeature | denotes | type 2B von Willebrand disease | D056728 |
| T4 | 99-102 | DiseaseOrPhenotypicFeature | denotes | VWD | D014842 |
Test-merged
| Id | Subject | Object | Predicate | Lexical cue | #label |
|---|---|---|---|---|---|
| T4 | 99-102 | DiseaseOrPhenotypicFeature | denotes | VWD | D014842 |
| T3 | 67-97 | DiseaseOrPhenotypicFeature | denotes | type 2B von Willebrand disease | D056728 |
| T2 | 25-39 | DiseaseOrPhenotypicFeature | denotes | genetic defect | DISEASE |
sentences
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| TextSentencer_T2 | 0-117 | Sentence | denotes | Clinical, laboratory and genetic defect of a Taiwanese family with type 2B von Willebrand disease (VWD) were studied. |
| T2 | 0-117 | Sentence | denotes | Clinical, laboratory and genetic defect of a Taiwanese family with type 2B von Willebrand disease (VWD) were studied. |
PubCasesORDO
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| AB1 | 75-97 | ORDO:903 | denotes | von Willebrand disease |