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PubMed:12471561 JSONTXT

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DisGeNET

Id Subject Object Predicate Lexical cue
T0 18-22 gene:1428 denotes CRYM
T1 54-75 disease:C3711374 denotes nonsyndromic deafness
T2 427-431 gene:1428 denotes CRYM
T3 457-478 disease:C3711374 denotes nonsyndromic deafness
T4 1427-1431 gene:1428 denotes CRYM
T5 1524-1545 disease:C3711374 denotes nonsyndromic deafness
R1 T0 T1 associated_with CRYM,nonsyndromic deafness
R2 T2 T3 associated_with CRYM,nonsyndromic deafness
R3 T4 T5 associated_with CRYM,nonsyndromic deafness

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
12471561-0#18#22#gene1428 18-22 gene1428 denotes CRYM
12471561-0#54#75#diseaseC3711374 54-75 diseaseC3711374 denotes nonsyndromic deafness
12471561-4#91#95#gene1428 1114-1118 gene1428 denotes CRYM
12471561-4#72#83#diseaseC3887505 1095-1106 diseaseC3887505 denotes dysfunction
18#22#gene142854#75#diseaseC3711374 12471561-0#18#22#gene1428 12471561-0#54#75#diseaseC3711374 associated_with CRYM,nonsyndromic deafness
91#95#gene142872#83#diseaseC3887505 12471561-4#91#95#gene1428 12471561-4#72#83#diseaseC3887505 associated_with CRYM,dysfunction