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Q28235848-54DB1E23-A487-4030-AF7D-F861F8C1850B
Q28235848-54DB1E23-A487-4030-AF7D-F861F8C1850B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28235848-54DB1E23-A487-4030-AF7D-F861F8C1850B
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
P433
Q28235848-54DB1E23-A487-4030-AF7D-F861F8C1850B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28235848-54DB1E23-A487-4030-AF7D-F861F8C1850B
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
469ac210a9bd89ef2e3c712e17fd2e431aca25d1
P433
12
http://www.w3.org/2001/XMLSchema#string