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Q28235848-FB467410-8953-4C76-B657-71E46E2E98E8
Q28235848-FB467410-8953-4C76-B657-71E46E2E98E8
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28235848-FB467410-8953-4C76-B657-71E46E2E98E8
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
P356
Q28235848-FB467410-8953-4C76-B657-71E46E2E98E8
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28235848-FB467410-8953-4C76-B657-71E46E2E98E8
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
0d868c5cf2b71db1c59c07aad5d8e26ca9b62117
469ac210a9bd89ef2e3c712e17fd2e431aca25d1
P356
10.1093/HMG/3.12.2175
http://www.w3.org/2001/XMLSchema#string
P356
3.12.2175