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PubMed:11810296 JSONTXT 5 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id Subject Object Predicate Lexical cue
T1 19-42 disease:C0152136 denotes normal tension glaucoma
T3 19-42 disease:C0152136 denotes normal tension glaucoma
T0 82-86 gene:4976 denotes OPA1
T2 82-86 gene:9968 denotes OPA1
T4 256-260 gene:9968 denotes OPA1
T6 256-260 gene:4976 denotes OPA1
T5 287-319 disease:C0338508 denotes autosomal dominant optic atrophy
T7 287-319 disease:C0338508 denotes autosomal dominant optic atrophy
T9 287-319 disease:C0338508 denotes autosomal dominant optic atrophy
T15 287-319 disease:C0338508 denotes autosomal dominant optic atrophy
T11 363-366 disease:C0152136 denotes NTG
T13 363-366 disease:C0152136 denotes NTG
T8 411-415 gene:4976 denotes OPA1
T10 411-415 gene:9968 denotes OPA1
T12 411-415 gene:4976 denotes OPA1
T14 411-415 gene:9968 denotes OPA1
T16 1559-1563 gene:4976 denotes OPA1
T18 1559-1563 gene:9968 denotes OPA1
T17 1589-1592 disease:C0152136 denotes NTG
T19 1589-1592 disease:C0152136 denotes NTG
R1 T0 T1 associated_with OPA1,normal tension glaucoma
R10 T18 T19 associated_with OPA1,NTG
R2 T2 T3 associated_with OPA1,normal tension glaucoma
R3 T4 T5 associated_with OPA1,autosomal dominant optic atrophy
R4 T6 T7 associated_with OPA1,autosomal dominant optic atrophy
R5 T8 T9 associated_with OPA1,autosomal dominant optic atrophy
R6 T10 T11 associated_with OPA1,NTG
R7 T12 T13 associated_with OPA1,NTG
R8 T14 T15 associated_with OPA1,autosomal dominant optic atrophy
R9 T16 T17 associated_with OPA1,NTG