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Q35629063-1F0373DA-0717-468B-99F6-EA505D9E967E
Q35629063-1F0373DA-0717-468B-99F6-EA505D9E967E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35629063-1F0373DA-0717-468B-99F6-EA505D9E967E
A recurrent mutation in GUCY2D associated with autosomal dominant cone dystrophy in a Chinese family
P2860
Q35629063-1F0373DA-0717-468B-99F6-EA505D9E967E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35629063-1F0373DA-0717-468B-99F6-EA505D9E967E
rank
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type
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Statement
wasDerivedFrom
b9482d167fb5cab04a148b51385209354ef67b24
P2860
Phenotype of autosomal dominant cone-rod dystrophy due to the R838C mutation of the GUCY2D gene encoding retinal guanylate cyclase-1.