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Q37458493-14035288-BFB6-4F25-B492-492470EA409F
Q37458493-14035288-BFB6-4F25-B492-492470EA409F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37458493-14035288-BFB6-4F25-B492-492470EA409F
Ca2+ dysregulation in Ryr1(I4895T/wt) mice causes congenital myopathy with progressive formation of minicores, cores, and nemaline rods
P2860
Q37458493-14035288-BFB6-4F25-B492-492470EA409F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37458493-14035288-BFB6-4F25-B492-492470EA409F
rank
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type
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Statement
wasDerivedFrom
0b1f07eacbb3202c7c39c44d8cdb994fd56ef3f7
P2860
A mutation in the transmembrane/luminal domain of the ryanodine receptor is associated with abnormal Ca2+ release channel function and severe central core disease.