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Q28235848-91FE4A7A-BFA6-489A-ACBA-0853172DF211
Q28235848-91FE4A7A-BFA6-489A-ACBA-0853172DF211
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28235848-91FE4A7A-BFA6-489A-ACBA-0853172DF211
Evidence for recessive as well as dominant forms of startle disease (hyperekplexia) caused by mutations in the alpha 1 subunit of the inhibitory glycine receptor
P577
Q28235848-91FE4A7A-BFA6-489A-ACBA-0853172DF211
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28235848-91FE4A7A-BFA6-489A-ACBA-0853172DF211
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
469ac210a9bd89ef2e3c712e17fd2e431aca25d1
P577
1994-12-01T00:00:00Z
http://www.w3.org/2001/XMLSchema#dateTime
P577
eb31caa6076664a5583bba79d31acfb7