PubMed:15041272 / 0-135
Annnotations
TEST-DiseaseOrPhenotypicFeature
| 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 |
Test-SequenceVariant
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 72-78 | SequenceVariant | denotes | R1306W |
Test-merged-2
| Id | Subject | Object | Predicate | Lexical cue | #label |
|---|---|---|---|---|---|
| T46254 | 72-78 | SequenceVariant | denotes | R1306W | |
| T1 | 36-66 | DiseaseOrPhenotypicFeature | denotes | type 2B von Willebrand disease | D056728 |
| T2 | 114-128 | DiseaseOrPhenotypicFeature | denotes | genetic defect | DISEASE |
Test-merged
| Id | Subject | Object | Predicate | Lexical cue | #label |
|---|---|---|---|---|---|
| T2 | 114-128 | DiseaseOrPhenotypicFeature | denotes | genetic defect | DISEASE |
| T1 | 36-66 | DiseaseOrPhenotypicFeature | denotes | type 2B von Willebrand disease | D056728 |
| T46254 | 72-78 | SequenceVariant | denotes | R1306W |
sentences
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| TextSentencer_T1 | 0-88 | Sentence | denotes | A first Taiwanese Chinese family of type 2B von Willebrand disease with R1306W mutation. |
| T1 | 0-88 | Sentence | denotes | A first Taiwanese Chinese family of type 2B von Willebrand disease with R1306W mutation. |
DisGeNET5_variant_disease
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| 15041272-0#72#78#geners61749384 | 72-78 | geners61749384 | denotes | R1306W |
| 15041272-0#36#66#diseaseC1282971 | 36-66 | diseaseC1282971 | denotes | type 2B von Willebrand disease |
| 72#78#geners6174938436#66#diseaseC1282971 | 15041272-0#72#78#geners61749384 | 15041272-0#36#66#diseaseC1282971 | associated_with | R1306W,type 2B von Willebrand disease |
PubCasesORDO
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| TI1 | 44-66 | ORDO:903 | denotes | von Willebrand disease |
tmVarCorpus
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 72-78 | ProteinMutation:p|SUB|R|1306|W | denotes | R1306W |