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PubMed:10189842 JSONTXT

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DisGeNET

Id Subject Object Predicate Lexical cue
T0 1486-1492 gene:1493 denotes CTLA-4
T1 1556-1571 disease:C0007570 denotes coeliac disease
R1 T0 T1 associated_with CTLA-4,coeliac disease

DisGeNET5_variant_disease

Id Subject Object Predicate Lexical cue
10189842-4#52#58#geners231775 543-549 geners231775 denotes 49 A/G
10189842-4#52#58#geners12722039 543-549 geners12722039 denotes 49 A/G
10189842-4#77#92#diseaseC0007570 568-583 diseaseC0007570 denotes coeliac disease
52#58#geners23177577#92#diseaseC0007570 10189842-4#52#58#geners231775 10189842-4#77#92#diseaseC0007570 associated_with 49 A/G,coeliac disease
52#58#geners1272203977#92#diseaseC0007570 10189842-4#52#58#geners12722039 10189842-4#77#92#diseaseC0007570 associated_with 49 A/G,coeliac disease

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
10189842-0#0#6#gene1493 506-512 gene1493 denotes CTLA-4
10189842-0#62#77#diseaseC0007570 1556-1571 diseaseC0007570 denotes coeliac disease
0#6#gene149362#77#diseaseC0007570 10189842-0#0#6#gene1493 10189842-0#62#77#diseaseC0007570 associated_with CTLA-4,coeliac disease

PMID_GLOBAL

Id Subject Object Predicate Lexical cue mondo_id
T1 62-77 DiseaseOrPhenotypicFeature denotes coeliac disease 0005130
T2 109-124 DiseaseOrPhenotypicFeature denotes coeliac disease 0005130
T3 568-583 DiseaseOrPhenotypicFeature denotes coeliac disease 0005130
T4 613-628 DiseaseOrPhenotypicFeature denotes coeliac disease 0005130
T5 891-906 DiseaseOrPhenotypicFeature denotes coeliac disease 0005130
T6 1556-1571 DiseaseOrPhenotypicFeature denotes coeliac disease 0005130