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Q43800108-F4998BBF-CD52-47D2-8F38-40485C593BFF
Q43800108-F4998BBF-CD52-47D2-8F38-40485C593BFF
BestRank
Statement
http://www.wikidata.org/entity/statement/Q43800108-F4998BBF-CD52-47D2-8F38-40485C593BFF
Familial and sporadic forms of central core disease are associated with mutations in the C-terminal domain of the skeletal muscle ryanodine receptor.
P2093
Q43800108-F4998BBF-CD52-47D2-8F38-40485C593BFF
BestRank
Statement
http://www.wikidata.org/entity/statement/Q43800108-F4998BBF-CD52-47D2-8F38-40485C593BFF
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
7ef577bd87b5ad0c6f6c6b90fa2b437096da4a4d
P1545
1
http://www.w3.org/2001/XMLSchema#string
P2093
Monnier N
http://www.w3.org/2001/XMLSchema#string