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Q37323334-CF254CA6-D518-4FD4-A473-2D7CA4CDCC35
Q37323334-CF254CA6-D518-4FD4-A473-2D7CA4CDCC35
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37323334-CF254CA6-D518-4FD4-A473-2D7CA4CDCC35
Usher syndromes due to MYO7A, PCDH15, USH2A or GPR98 mutations share retinal disease mechanism.
P2860
Q37323334-CF254CA6-D518-4FD4-A473-2D7CA4CDCC35
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37323334-CF254CA6-D518-4FD4-A473-2D7CA4CDCC35
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
ed06be1eb59d39ae3f839a4f558e9562e0a583d5
P2860
Stable rhodopsin/arrestin complex leads to retinal degeneration in a transgenic mouse model of autosomal dominant retinitis pigmentosa.