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PubMed:17911039 JSONTXT

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PubmedHPO

Id Subject Object Predicate Lexical cue
T1 162-181 HP_0000007 denotes autosomal recessive
T2 330-351 HP_0000846 denotes adrenal insufficiency
T3 353-362 HP_0002571 denotes achalasia
T4 368-376 HP_0000522 denotes alacrima
T1 162-181 HP_0000007 denotes autosomal recessive
T2 330-351 HP_0000846 denotes adrenal insufficiency
T3 353-362 HP_0002571 denotes achalasia
T4 368-376 HP_0000522 denotes alacrima

DisGeNET

Id Subject Object Predicate Lexical cue
T0 93-97 gene:8086 denotes AAAS
T1 119-136 disease:C0271742 denotes triple A syndrome
T2 235-239 gene:8086 denotes AAAS
T3 138-155 disease:C0271742 denotes Triple A syndrome
T4 1166-1170 gene:8086 denotes AAAS
T5 1190-1207 disease:C0271742 denotes Triple A syndrome
R1 T0 T1 associated_with AAAS,triple A syndrome
R2 T2 T3 associated_with AAAS,Triple A syndrome
R3 T4 T5 associated_with AAAS,Triple A syndrome

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
17911039-0#93#97#gene8086 93-97 gene8086 denotes AAAS
17911039-0#119#136#diseaseC0271742 119-136 diseaseC0271742 denotes triple A syndrome
17911039-1#97#101#gene8086 235-239 gene8086 denotes AAAS
17911039-1#24#52#diseaseC3899988 162-190 diseaseC3899988 denotes autosomal recessive disorder
93#97#gene8086119#136#diseaseC0271742 17911039-0#93#97#gene8086 17911039-0#119#136#diseaseC0271742 associated_with AAAS,triple A syndrome
97#101#gene808624#52#diseaseC3899988 17911039-1#97#101#gene8086 17911039-1#24#52#diseaseC3899988 associated_with AAAS,autosomal recessive disorder