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PubMed:17517692 JSONTXT

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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