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Q36460971-C06472F7-B3E1-4B9C-B8D4-6143BB279889
Q36460971-C06472F7-B3E1-4B9C-B8D4-6143BB279889
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36460971-C06472F7-B3E1-4B9C-B8D4-6143BB279889
A mutation in the transmembrane/luminal domain of the ryanodine receptor is associated with abnormal Ca2+ release channel function and severe central core disease.
P1476
Q36460971-C06472F7-B3E1-4B9C-B8D4-6143BB279889
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36460971-C06472F7-B3E1-4B9C-B8D4-6143BB279889
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
19758012e415735fb0530a2819c646ff0952114a
P1476
A mutation in the transmembran
......
d severe central core disease.
@en