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Q52317562-D75D5B89-C276-4875-B5C4-77A58342B05F
Q52317562-D75D5B89-C276-4875-B5C4-77A58342B05F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q52317562-D75D5B89-C276-4875-B5C4-77A58342B05F
BEST1 protein stability and degradation pathways differ between autosomal dominant Best disease and autosomal recessive bestrophinopathy accounting for the distinct retinal phenotypes.
P2860
Q52317562-D75D5B89-C276-4875-B5C4-77A58342B05F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q52317562-D75D5B89-C276-4875-B5C4-77A58342B05F
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
a317b534dfdd8969cfa09b7c9f4dc21ed8420864
P2860
Disease-causing mutations in BEST1 gene are associated with altered sorting of bestrophin-1 protein.