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Q36460971-E303FD4D-0F47-4F18-9A77-4BBF7661D4AC
Q36460971-E303FD4D-0F47-4F18-9A77-4BBF7661D4AC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36460971-E303FD4D-0F47-4F18-9A77-4BBF7661D4AC
A mutation in the transmembrane/luminal domain of the ryanodine receptor is associated with abnormal Ca2+ release channel function and severe central core disease.
P932
Q36460971-E303FD4D-0F47-4F18-9A77-4BBF7661D4AC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36460971-E303FD4D-0F47-4F18-9A77-4BBF7661D4AC
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
19758012e415735fb0530a2819c646ff0952114a
P932
22438
http://www.w3.org/2001/XMLSchema#string