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Q41928481-221FCED2-9A23-4E5A-A666-3EF6202EED84
Q41928481-221FCED2-9A23-4E5A-A666-3EF6202EED84
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41928481-221FCED2-9A23-4E5A-A666-3EF6202EED84
A novel syndrome of Klippel-Feil anomaly, myopathy, and characteristic facies is linked to a null mutation in MYO18B.
P2860
Q41928481-221FCED2-9A23-4E5A-A666-3EF6202EED84
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41928481-221FCED2-9A23-4E5A-A666-3EF6202EED84
rank
NormalRank
type
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Statement
wasDerivedFrom
d2c75167dcd80bf27ce1c5126d1b4ec100be42d5
P2860
MYO18B, a candidate tumor suppressor gene at chromosome 22q12.1, deleted, mutated, and methylated in human lung cancer.