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Q52317562-0676EFFB-E22E-49AE-B20D-175532F2C209
Q52317562-0676EFFB-E22E-49AE-B20D-175532F2C209
BestRank
Statement
http://www.wikidata.org/entity/statement/Q52317562-0676EFFB-E22E-49AE-B20D-175532F2C209
BEST1 protein stability and degradation pathways differ between autosomal dominant Best disease and autosomal recessive bestrophinopathy accounting for the distinct retinal phenotypes.
P2860
Q52317562-0676EFFB-E22E-49AE-B20D-175532F2C209
BestRank
Statement
http://www.wikidata.org/entity/statement/Q52317562-0676EFFB-E22E-49AE-B20D-175532F2C209
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
a317b534dfdd8969cfa09b7c9f4dc21ed8420864
P2860
Autosomal Recessive Bestrophinopathy Is Not Associated With the Loss of Bestrophin-1 Anion Channel Function in a Patient With a Novel BEST1 Mutation