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Q39364834-1C225D86-3CAA-4D49-BB11-FA335E73AFBF
Q39364834-1C225D86-3CAA-4D49-BB11-FA335E73AFBF
BestRank
Statement
http://www.wikidata.org/entity/statement/Q39364834-1C225D86-3CAA-4D49-BB11-FA335E73AFBF
Isolated late-onset cone-rod dystrophy revealing a familial neurogenic muscle weakness, ataxia, and retinitis pigmentosa syndrome with the T8993G mitochondrial mutation.
P356
Q39364834-1C225D86-3CAA-4D49-BB11-FA335E73AFBF
BestRank
Statement
http://www.wikidata.org/entity/statement/Q39364834-1C225D86-3CAA-4D49-BB11-FA335E73AFBF
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
b65afc210436386f8df5d9b62b014247ffc34a5a
P356
10.1016/S0002-9394(01)01187-4
http://www.w3.org/2001/XMLSchema#string
P356
S0002-9394(01)01187-4