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Q28235848-3F9C4C71-729C-4B13-9C95-68AEC38AD15E
Q28235848-3F9C4C71-729C-4B13-9C95-68AEC38AD15E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28235848-3F9C4C71-729C-4B13-9C95-68AEC38AD15E
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
P50
Q28235848-3F9C4C71-729C-4B13-9C95-68AEC38AD15E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28235848-3F9C4C71-729C-4B13-9C95-68AEC38AD15E
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
469ac210a9bd89ef2e3c712e17fd2e431aca25d1
P1545
1
http://www.w3.org/2001/XMLSchema#string
P50
Mark I Rees