awgldk
/
wikidata
/
Login
Register
TriplyDB
Wikidata
Browser
Table
SPARQL
Graphs
1
1
Services
1
1
Assets
0
0
Insights
Schema
BETA
Class frequency
Class hierarchy
Q28189818-16F3CC50-5B8D-4E46-86BD-9417BC814D9D
Q28189818-16F3CC50-5B8D-4E46-86BD-9417BC814D9D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28189818-16F3CC50-5B8D-4E46-86BD-9417BC814D9D
Isoform heterogeneity of the human gephyrin gene (GPHN), binding domains to the glycine receptor, and mutation analysis in hyperekplexia
P2860
Q28189818-16F3CC50-5B8D-4E46-86BD-9417BC814D9D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28189818-16F3CC50-5B8D-4E46-86BD-9417BC814D9D
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
d576f9837777642ce0110a8986bf6e24690be4fd
P2860
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