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
Q28078420-5E6521BE-E201-4191-9A23-27169D258D2B
Q28078420-5E6521BE-E201-4191-9A23-27169D258D2B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28078420-5E6521BE-E201-4191-9A23-27169D258D2B
Review of RyR1 pathway and associated pathomechanisms
P2860
Q28078420-5E6521BE-E201-4191-9A23-27169D258D2B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28078420-5E6521BE-E201-4191-9A23-27169D258D2B
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
937d7f4e6d3ac7118402e21955c4608fd200da05
P2860
An autosomal dominant congenital myopathy with cores and rods is associated with a neomutation in the RYR1 gene encoding the skeletal muscle ryanodine receptor.