PubMed:17517692
Annnotations
DisGeNET
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T0 | 687-691 | gene:54880 | denotes | BCOR |
T1 | 826-839 | disease:C1846265 | denotes | OFCD syndrome |
R1 | T0 | T1 | associated_with | BCOR,OFCD syndrome |
PubmedHPO
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 162-170 | HP_0001417 | denotes | X-linked |
T2 | 206-228 | HP_0001671 | denotes | cardiac septal defects |
T1 | 162-170 | HP_0001417 | denotes | X-linked |
T2 | 206-228 | HP_0001671 | denotes | cardiac septal defects |
T3 | 214-228 | HP_0001671 | denotes | septal defects |
T4 | 252-268 | HP_0000164 | denotes | dental anomalies |
T5 | 542-554 | HP_0001651 | denotes | dextrocardia |
T6 | 556-564 | HP_0001746 | denotes | asplenia |
T7 | 569-591 | HP_0002566 | denotes | intestinal malrotation |
T8 | 580-591 | HP_0002566 | denotes | malrotation |
T9 | 1247-1261 | HP_0000568 | denotes | microphthalmia |
T10 | 1266-1274 | HP_0000589 | denotes | coloboma |
T3 | 214-228 | HP_0001671 | denotes | septal defects |
T4 | 252-268 | HP_0000164 | denotes | dental anomalies |
T5 | 542-554 | HP_0001651 | denotes | dextrocardia |
T6 | 556-564 | HP_0001746 | denotes | asplenia |
T7 | 569-591 | HP_0002566 | denotes | intestinal malrotation |
T8 | 580-591 | HP_0002566 | denotes | malrotation |
T9 | 1247-1261 | HP_0000568 | denotes | microphthalmia |
T10 | 1266-1274 | HP_0000589 | denotes | coloboma |
DisGeNET5_gene_disease
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
17517692-4#25#29#gene54880 | 687-691 | gene54880 | denotes | BCOR |
17517692-4#164#177#diseaseC1846265 | 826-839 | diseaseC1846265 | denotes | OFCD syndrome |
25#29#gene54880164#177#diseaseC1846265 | 17517692-4#25#29#gene54880 | 17517692-4#164#177#diseaseC1846265 | associated_with | BCOR,OFCD syndrome |