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Q28284847-1D095D9D-4ACD-4B3F-8AF0-26ABAFD8A0BE
Q28284847-1D095D9D-4ACD-4B3F-8AF0-26ABAFD8A0BE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28284847-1D095D9D-4ACD-4B3F-8AF0-26ABAFD8A0BE
K7del is a common TPM2 gene mutation associated with nemaline myopathy and raised myofibre calcium sensitivity
P478
Q28284847-1D095D9D-4ACD-4B3F-8AF0-26ABAFD8A0BE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28284847-1D095D9D-4ACD-4B3F-8AF0-26ABAFD8A0BE
rank
NormalRank
type
BestRank
Statement
P478
136
http://www.w3.org/2001/XMLSchema#string