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Q41928481-EE11463E-3A6F-41CA-BADD-39D0D5EEA962
Q41928481-EE11463E-3A6F-41CA-BADD-39D0D5EEA962
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41928481-EE11463E-3A6F-41CA-BADD-39D0D5EEA962
A novel syndrome of Klippel-Feil anomaly, myopathy, and characteristic facies is linked to a null mutation in MYO18B.
P2093
Q41928481-EE11463E-3A6F-41CA-BADD-39D0D5EEA962
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41928481-EE11463E-3A6F-41CA-BADD-39D0D5EEA962
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
0cce053421955450eec38eb32b50a8b29521bbd8
P1545
4
http://www.w3.org/2001/XMLSchema#string
P2093
Jawahir Y Mohamed
http://www.w3.org/2001/XMLSchema#string