wikimedia
/
wikidata
/
Login
Register
TriplyDB
Wikidata
Browser
Table
SPARQL
Graphs
1
1
Services
1
1
Assets
0
0
Insights
Schema
BETA
Class frequency
Class hierarchy
Q37458493-6B57B518-53C7-493F-8976-C7A704EEB374
Q37458493-6B57B518-53C7-493F-8976-C7A704EEB374
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37458493-6B57B518-53C7-493F-8976-C7A704EEB374
Ca2+ dysregulation in Ryr1(I4895T/wt) mice causes congenital myopathy with progressive formation of minicores, cores, and nemaline rods
P2860
Q37458493-6B57B518-53C7-493F-8976-C7A704EEB374
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37458493-6B57B518-53C7-493F-8976-C7A704EEB374
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
52b45f35f184e486ea9064cf422d36aaaf6bcf16
P2860
A homozygous splicing mutation causing a depletion of skeletal muscle RYR1 is associated with multi-minicore disease congenital myopathy with ophthalmoplegia.