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Q39364834-AAF2726A-338E-4628-8E0D-FA3C4166F870
Q39364834-AAF2726A-338E-4628-8E0D-FA3C4166F870
BestRank
Statement
http://www.wikidata.org/entity/statement/Q39364834-AAF2726A-338E-4628-8E0D-FA3C4166F870
Isolated late-onset cone-rod dystrophy revealing a familial neurogenic muscle weakness, ataxia, and retinitis pigmentosa syndrome with the T8993G mitochondrial mutation.
P698
Q39364834-AAF2726A-338E-4628-8E0D-FA3C4166F870
BestRank
Statement
http://www.wikidata.org/entity/statement/Q39364834-AAF2726A-338E-4628-8E0D-FA3C4166F870
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
b65afc210436386f8df5d9b62b014247ffc34a5a
P698
11730668
http://www.w3.org/2001/XMLSchema#string