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Q28235848-8ACF3B44-8B47-4ADE-BDDB-9D8057C2BA14
Q28235848-8ACF3B44-8B47-4ADE-BDDB-9D8057C2BA14
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28235848-8ACF3B44-8B47-4ADE-BDDB-9D8057C2BA14
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
P698
Q28235848-8ACF3B44-8B47-4ADE-BDDB-9D8057C2BA14
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28235848-8ACF3B44-8B47-4ADE-BDDB-9D8057C2BA14
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
0d868c5cf2b71db1c59c07aad5d8e26ca9b62117
469ac210a9bd89ef2e3c712e17fd2e431aca25d1
P698
7881416
http://www.w3.org/2001/XMLSchema#string