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PubMed:1775314 JSONTXT

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DisGeNET

Id Subject Object Predicate Lexical cue
T0 149-158 gene:6010 denotes rhodopsin
T1 264-266 disease:C0339525 denotes RP
T2 149-158 gene:6010 denotes rhodopsin
T3 223-262 disease:C0339525 denotes autosomal dominant retinitis pigmentosa
T4 860-869 gene:6010 denotes rhodopsin
T5 957-977 disease:C0035304 denotes retinal degeneration
T6 860-869 gene:6010 denotes rhodopsin
T7 881-883 disease:C0339525 denotes RP
R1 T0 T1 associated_with rhodopsin,RP
R2 T2 T3 associated_with rhodopsin,autosomal dominant retinitis pigmentosa
R3 T4 T5 associated_with rhodopsin,retinal degeneration
R4 T6 T7 associated_with rhodopsin,RP

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 223-241 HP_0000006 denotes autosomal dominant
T2 499-519 HP_0000546 denotes retinal degeneration
T3 957-977 HP_0000546 denotes retinal degeneration

DisGeNET5_variant_disease

Id Subject Object Predicate Lexical cue
1775314-5#34#44#geners104893768 849-859 geners104893768 denotes Pro-23-His
1775314-5#66#68#diseaseC0339525 881-883 diseaseC0339525 denotes RP
34#44#geners10489376866#68#diseaseC0339525 1775314-5#34#44#geners104893768 1775314-5#66#68#diseaseC0339525 associated_with Pro-23-His,RP

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
1775314-5#45#54#gene6010 860-869 gene6010 denotes rhodopsin
1775314-5#66#68#diseaseC0339525 881-883 diseaseC0339525 denotes RP
45#54#gene601066#68#diseaseC0339525 1775314-5#45#54#gene6010 1775314-5#66#68#diseaseC0339525 associated_with rhodopsin,RP