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PubMed:18987194 JSONTXT

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PMID_GLOBAL

Id Subject Object Predicate Lexical cue mondo_id
T1 397-400 DiseaseOrPhenotypicFeature denotes fed 0007620
T2 514-523 DiseaseOrPhenotypicFeature denotes sensitive 0000605

DisGeNET

Id Subject Object Predicate Lexical cue
T0 1553-1556 gene:8767 denotes CCK
T1 1437-1445 disease:C0085648 denotes ganglion
T2 1553-1556 gene:8767 denotes CCK
T3 1437-1445 disease:C1258666 denotes ganglion
T4 1553-1556 gene:885 denotes CCK
T5 1437-1445 disease:C0085648 denotes ganglion
T6 1553-1556 gene:885 denotes CCK
T7 1437-1445 disease:C1258666 denotes ganglion
R1 T0 T1 associated_with CCK,ganglion
R2 T2 T3 associated_with CCK,ganglion
R3 T4 T5 associated_with CCK,ganglion
R4 T6 T7 associated_with CCK,ganglion

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
18987194-8#181#184#gene885 1553-1556 gene885 denotes CCK
18987194-8#65#73#diseaseC0085648 1437-1445 diseaseC0085648 denotes ganglion
18987194-8#65#73#diseaseC1258666 1437-1445 diseaseC1258666 denotes ganglion
181#184#gene88565#73#diseaseC0085648 18987194-8#181#184#gene885 18987194-8#65#73#diseaseC0085648 associated_with CCK,ganglion
181#184#gene88565#73#diseaseC1258666 18987194-8#181#184#gene885 18987194-8#65#73#diseaseC1258666 associated_with CCK,ganglion