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PubMed:10037069 JSONTXT

Annnotations TAB JSON ListView MergeView

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 316-331 HP_0100647 denotes Graves' disease

DisGeNET5_variant_disease

Id Subject Object Predicate Lexical cue
10037069-2#287#291#geners2234919 590-594 geners2234919 denotes P52T
10037069-2#14#29#diseaseC0018213 316-331 diseaseC0018213 denotes Graves' disease
287#291#geners223491914#29#diseaseC0018213 10037069-2#287#291#geners2234919 10037069-2#14#29#diseaseC0018213 associated_with P52T,Graves' disease

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
10037069-2#292#296#gene7253 595-599 gene7253 denotes TSHR
10037069-2#14#29#diseaseC0018213 316-331 diseaseC0018213 denotes Graves' disease
292#296#gene725314#29#diseaseC0018213 10037069-2#292#296#gene7253 10037069-2#14#29#diseaseC0018213 associated_with TSHR,Graves' disease