PubMed:17495183 / 1505-1508
Annnotations
TEST-DiseaseOrPhenotypicFeature
| Id | Subject | Object | Predicate | Lexical cue | #label |
|---|---|---|---|---|---|
| T18 | 0-3 | DiseaseOrPhenotypicFeature | denotes | T2D | D003924 |
Test-SequenceVariant
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T13 | 0-3 | SequenceVariant | denotes | T2D |
Test-merged-2
| Id | Subject | Object | Predicate | Lexical cue | #label |
|---|---|---|---|---|---|
| T78077 | 0-3 | SequenceVariant | denotes | T2D | |
| T18 | 0-3 | DiseaseOrPhenotypicFeature | denotes | T2D | D003924 |
Test-merged
| Id | Subject | Object | Predicate | Lexical cue | #label |
|---|---|---|---|---|---|
| T18 | 0-3 | DiseaseOrPhenotypicFeature | denotes | T2D | D003924 |
DisGeNET
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T3 | 0-3 | disease:C0011860 | denotes | T2D |
DisGeNET5_gene_disease
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| 17495183-10#136#139#diseaseC0011860 | 0-3 | diseaseC0011860 | denotes | T2D |