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Q24308692-33B94CBD-31AB-4595-8043-ADD7C9CDEE6F
Q24308692-33B94CBD-31AB-4595-8043-ADD7C9CDEE6F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24308692-33B94CBD-31AB-4595-8043-ADD7C9CDEE6F
Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome
P2860
Q24308692-33B94CBD-31AB-4595-8043-ADD7C9CDEE6F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24308692-33B94CBD-31AB-4595-8043-ADD7C9CDEE6F
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
6aa0097cad2c4a8fa5404562a1660b76ae9295c9
P2860
Dysfunctional cilia lead to altered ependyma and choroid plexus function, and result in the formation of hydrocephalus.