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PubMed:23209189 JSONTXT

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DisGeNET

Id Subject Object Predicate Lexical cue
T0 882-890 gene:22930 denotes RAB3GAP1
T1 924-944 disease:C0027765 denotes neurologic disorders
T2 895-900 gene:130013 denotes ACMSD
T3 924-944 disease:C0027765 denotes neurologic disorders
R1 T0 T1 associated_with RAB3GAP1,neurologic disorders
R2 T2 T3 associated_with ACMSD,neurologic disorders

Allie

Id Subject Object Predicate Lexical cue
SS1_23209189_1_0 209-224 expanded denotes type 2 diabetes
SS2_23209189_1_0 226-229 abbr denotes T2D
AE1_23209189_1_0 SS1_23209189_1_0 SS2_23209189_1_0 abbreviatedTo type 2 diabetes,T2D

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 767-785 HP_0000855 denotes insulin resistance
T2 912-934 HP_0000707 denotes involved in neurologic
T3 924-944 HP_0000707 denotes neurologic disorders

DisGeNET5_variant_disease

Id Subject Object Predicate Lexical cue
23209189-3#89#98#geners6723108 439-448 geners6723108 denotes rs6723108
23209189-3#20#35#diseaseC0011860 370-385 diseaseC0011860 denotes type 2 diabetes
89#98#geners672310820#35#diseaseC0011860 23209189-3#89#98#geners6723108 23209189-3#20#35#diseaseC0011860 associated_with rs6723108,type 2 diabetes

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
23209189-6#29#37#gene22930 882-890 gene22930 denotes RAB3GAP1
23209189-6#42#47#gene130013 895-900 gene130013 denotes ACMSD
23209189-6#71#91#diseaseC0027765 924-944 diseaseC0027765 denotes neurologic disorders
29#37#gene2293071#91#diseaseC0027765 23209189-6#29#37#gene22930 23209189-6#71#91#diseaseC0027765 associated_with RAB3GAP1,neurologic disorders
42#47#gene13001371#91#diseaseC0027765 23209189-6#42#47#gene130013 23209189-6#71#91#diseaseC0027765 associated_with ACMSD,neurologic disorders