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PubMed:3722385 JSONTXT

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DisGeNET

Id Subject Object Predicate Lexical cue
T0 68-78 gene:7276 denotes prealbumin
T1 95-117 disease:C0206246 denotes hereditary amyloidosis
R1 T0 T1 associated_with prealbumin,hereditary amyloidosis

DisGeNET5_variant_disease

Id Subject Object Predicate Lexical cue
3722385-4#144#180#geners11541794 755-791 geners11541794 denotes alanine for threonine at position 60
3722385-4#25#32#diseaseC0002726 636-643 diseaseC0002726 denotes amyloid
144#180#geners1154179425#32#diseaseC0002726 3722385-4#144#180#geners11541794 3722385-4#25#32#diseaseC0002726 associated_with alanine for threonine at position 60,amyloid

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
3722385-0#68#78#gene7276 68-78 gene7276 denotes prealbumin
3722385-0#95#117#diseaseC0206246 95-117 diseaseC0206246 denotes hereditary amyloidosis
3722385-4#65#75#gene7276 676-686 gene7276 denotes prealbumin
3722385-4#25#32#diseaseC0002726 636-643 diseaseC0002726 denotes amyloid
68#78#gene727695#117#diseaseC0206246 3722385-0#68#78#gene7276 3722385-0#95#117#diseaseC0206246 associated_with prealbumin,hereditary amyloidosis
65#75#gene727625#32#diseaseC0002726 3722385-4#65#75#gene7276 3722385-4#25#32#diseaseC0002726 associated_with prealbumin,amyloid