PubMed:17000021 / 789-792
Annnotations
TEST-DiseaseOrPhenotypicFeature
| Id | Subject | Object | Predicate | Lexical cue | #label |
|---|---|---|---|---|---|
| T8 | 0-3 | DiseaseOrPhenotypicFeature | denotes | T1D | D003922 |
Test-SequenceVariant
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T4 | 0-3 | SequenceVariant | denotes | T1D |
Test-merged-2
| Id | Subject | Object | Predicate | Lexical cue | #label |
|---|---|---|---|---|---|
| T12775 | 0-3 | SequenceVariant | denotes | T1D | |
| T8 | 0-3 | DiseaseOrPhenotypicFeature | denotes | T1D | D003922 |
Test-merged
| Id | Subject | Object | Predicate | Lexical cue | #label |
|---|---|---|---|---|---|
| T8 | 0-3 | DiseaseOrPhenotypicFeature | denotes | T1D | D003922 |
DisGeNET
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 0-3 | disease:C0011854 | denotes | T1D |