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PubMed:9931337 JSONTXT

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DisGeNET

Id Subject Object Predicate Lexical cue
T0 121-124 gene:1406 denotes CRX
T1 0-26 disease:C0339527 denotes Leber congenital amaurosis
T2 165-168 gene:1406 denotes CRX
T3 0-26 disease:C0339527 denotes Leber congenital amaurosis
R1 T0 T1 associated_with CRX,Leber congenital amaurosis
R2 T2 T3 associated_with CRX,Leber congenital amaurosis

DisGeNET5_variant_disease

Id Subject Object Predicate Lexical cue
9931337-0#60#64#geners104894673 60-64 geners104894673 denotes R90W
9931337-0#0#26#diseaseC0339527 0-26 diseaseC0339527 denotes Leber congenital amaurosis
9931337-10#28#32#geners104894673 1561-1565 geners104894673 denotes R90W
9931337-10#226#250#diseaseC1301509 1759-1783 diseaseC1301509 denotes severe visual impairment
9931337-10#254#257#diseaseC2931258 1787-1790 diseaseC2931258 denotes LCA
60#64#geners1048946730#26#diseaseC0339527 9931337-0#60#64#geners104894673 9931337-0#0#26#diseaseC0339527 associated_with R90W,Leber congenital amaurosis
28#32#geners104894673226#250#diseaseC1301509 9931337-10#28#32#geners104894673 9931337-10#226#250#diseaseC1301509 associated_with R90W,severe visual impairment
28#32#geners104894673254#257#diseaseC2931258 9931337-10#28#32#geners104894673 9931337-10#254#257#diseaseC2931258 associated_with R90W,LCA

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
9931337-0#121#124#gene1406 121-124 gene1406 denotes CRX
9931337-0#165#168#gene1406 165-168 gene1406 denotes CRX
9931337-0#0#26#diseaseC0339527 0-26 diseaseC0339527 denotes Leber congenital amaurosis
9931337-10#28#32#gene1406 1561-1565 gene1406 denotes R90W
9931337-10#55#58#gene1406 1588-1591 gene1406 denotes CRX
9931337-10#226#250#diseaseC1301509 1759-1783 diseaseC1301509 denotes severe visual impairment
9931337-10#254#257#diseaseC2931258 1787-1790 diseaseC2931258 denotes LCA
9931337-10#226#250#diseaseC1301509 1759-1783 diseaseC1301509 denotes severe visual impairment
9931337-10#254#257#diseaseC2931258 1787-1790 diseaseC2931258 denotes LCA
9931337-2#22#25#gene1406 392-395 gene1406 denotes CRX
9931337-2#85#103#diseaseC0035334 455-473 diseaseC0035334 denotes cone-rod dystrophy
9931337-2#105#109#diseaseC0035334 475-479 diseaseC0035334 denotes CORD
121#124#gene14060#26#diseaseC0339527 9931337-0#121#124#gene1406 9931337-0#0#26#diseaseC0339527 associated_with CRX,Leber congenital amaurosis
165#168#gene14060#26#diseaseC0339527 9931337-0#165#168#gene1406 9931337-0#0#26#diseaseC0339527 associated_with CRX,Leber congenital amaurosis
28#32#gene1406226#250#diseaseC1301509 9931337-10#28#32#gene1406 9931337-10#226#250#diseaseC1301509 associated_with R90W,severe visual impairment
28#32#gene1406254#257#diseaseC2931258 9931337-10#28#32#gene1406 9931337-10#254#257#diseaseC2931258 associated_with R90W,LCA
28#32#gene1406226#250#diseaseC1301509 9931337-10#28#32#gene1406 9931337-10#226#250#diseaseC1301509 associated_with R90W,severe visual impairment
28#32#gene1406254#257#diseaseC2931258 9931337-10#28#32#gene1406 9931337-10#254#257#diseaseC2931258 associated_with R90W,LCA
55#58#gene1406226#250#diseaseC1301509 9931337-10#55#58#gene1406 9931337-10#226#250#diseaseC1301509 associated_with CRX,severe visual impairment
55#58#gene1406254#257#diseaseC2931258 9931337-10#55#58#gene1406 9931337-10#254#257#diseaseC2931258 associated_with CRX,LCA
55#58#gene1406226#250#diseaseC1301509 9931337-10#55#58#gene1406 9931337-10#226#250#diseaseC1301509 associated_with CRX,severe visual impairment
55#58#gene1406254#257#diseaseC2931258 9931337-10#55#58#gene1406 9931337-10#254#257#diseaseC2931258 associated_with CRX,LCA
22#25#gene140685#103#diseaseC0035334 9931337-2#22#25#gene1406 9931337-2#85#103#diseaseC0035334 associated_with CRX,cone-rod dystrophy
22#25#gene1406105#109#diseaseC0035334 9931337-2#22#25#gene1406 9931337-2#105#109#diseaseC0035334 associated_with CRX,CORD