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Q41928481-8D614A82-1DFE-4CB1-A9B7-A2665D42C2AB
Q41928481-8D614A82-1DFE-4CB1-A9B7-A2665D42C2AB
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41928481-8D614A82-1DFE-4CB1-A9B7-A2665D42C2AB
A novel syndrome of Klippel-Feil anomaly, myopathy, and characteristic facies is linked to a null mutation in MYO18B.
P2860
Q41928481-8D614A82-1DFE-4CB1-A9B7-A2665D42C2AB
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41928481-8D614A82-1DFE-4CB1-A9B7-A2665D42C2AB
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
d2c75167dcd80bf27ce1c5126d1b4ec100be42d5
P2860
Cardiomyopathy: a systematic review of disease-causing mutations in myosin heavy chain 7 and their phenotypic manifestations.