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Q44832235-3594EAE5-319B-4C47-95CF-1B362DCB5EE1
Q44832235-3594EAE5-319B-4C47-95CF-1B362DCB5EE1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q44832235-3594EAE5-319B-4C47-95CF-1B362DCB5EE1
A novel hyperekplexia-causing mutation in the pre-transmembrane segment 1 of the human glycine receptor alpha1 subunit reduces membrane expression and impairs gating by agonists.
P2860
Q44832235-3594EAE5-319B-4C47-95CF-1B362DCB5EE1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q44832235-3594EAE5-319B-4C47-95CF-1B362DCB5EE1
rank
NormalRank
type
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Statement
wasDerivedFrom
601fa967d57908ad3e3ee184d95281b8f4086a6c
P2860
Startle disease, or hyperekplexia: response to clonazepam and assignment of the gene (STHE) to chromosome 5q by linkage analysis