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PubMed:10586248 / 187-198 JSONTXT

Annnotations TAB JSON ListView MergeView

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
10586248-1#62#73#diseaseC0007682 0-11 diseaseC0007682 denotes CNS disease
10586248-1#62#73#diseaseC0007682 0-11 diseaseC0007682 denotes CNS disease
10586248-1#62#73#diseaseC0007682 0-11 diseaseC0007682 denotes CNS disease
10586248-1#62#73#diseaseC0007682 0-11 diseaseC0007682 denotes CNS disease

DisGeNet-2017-sample

Id Subject Object Predicate Lexical cue
T937 0-11 disease:C0007682 denotes CNS disease

DisGeNET

Id Subject Object Predicate Lexical cue
T1 0-11 disease:C0007682 denotes CNS disease
T3 0-11 disease:C0007682 denotes CNS disease
T5 0-11 disease:C0007682 denotes CNS disease
T7 0-11 disease:C0007682 denotes CNS disease
T17 0-11 disease:C0007682 denotes CNS disease
T21 0-11 disease:C0007682 denotes CNS disease
T25 0-11 disease:C0007682 denotes CNS disease