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PubMed:10196695 JSONTXT

Annnotations TAB JSON ListView MergeView

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 122-149 HP_0000707 denotes neurodevelopmental disorder
T2 933-957 HP_0001466 denotes contiguous gene syndrome

DisGeNET

Id Subject Object Predicate Lexical cue
T0 587-592 gene:7337 denotes UBE3A
T1 634-636 disease:C0162635 denotes AS
R1 T0 T1 associated_with UBE3A,AS

BioLarkPubmedHPO

Id Subject Object Predicate Lexical cue
HP:0000707 122-149 HP:0000707 denotes neurodevelopmental disorder
HP:0001466 933-957 HP:0001466 denotes contiguous gene syndrome
T1 122-149 HP:0000707 denotes neurodevelopmental disorder
T2 933-957 HP:0001466 denotes contiguous gene syndrome
T1 122-149 HP:0000707 denotes neurodevelopmental disorder
T2 933-957 HP:0001466 denotes contiguous gene syndrome
T1 122-149 HP:0000707 denotes neurodevelopmental disorder
T2 933-957 HP:0001466 denotes contiguous gene syndrome

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
10196695-3#13#18#gene7337 587-592 gene7337 denotes UBE3A
10196695-3#60#62#diseaseC0162635 634-636 diseaseC0162635 denotes AS
13#18#gene733760#62#diseaseC0162635 10196695-3#13#18#gene7337 10196695-3#60#62#diseaseC0162635 associated_with UBE3A,AS