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
Q24617292-F3B3644B-36AE-4A5F-B905-77A0D224CB4A
Q24617292-F3B3644B-36AE-4A5F-B905-77A0D224CB4A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24617292-F3B3644B-36AE-4A5F-B905-77A0D224CB4A
Mutations of the selenoprotein N gene, which is implicated in rigid spine muscular dystrophy, cause the classical phenotype of multiminicore disease: reassessing the nosology of early-onset myopathies
P2860
Q24617292-F3B3644B-36AE-4A5F-B905-77A0D224CB4A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24617292-F3B3644B-36AE-4A5F-B905-77A0D224CB4A
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
33820fd8f5efa860c546beed01032fc0c45f0fb9
P2860
Ca2+ marks: miniature calcium signals in single mitochondria driven by ryanodine receptors