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Q41928481-05BD1BCE-2CA2-41A9-B635-F3125829713C
Q41928481-05BD1BCE-2CA2-41A9-B635-F3125829713C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41928481-05BD1BCE-2CA2-41A9-B635-F3125829713C
A novel syndrome of Klippel-Feil anomaly, myopathy, and characteristic facies is linked to a null mutation in MYO18B.
P356
Q41928481-05BD1BCE-2CA2-41A9-B635-F3125829713C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41928481-05BD1BCE-2CA2-41A9-B635-F3125829713C
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
0cce053421955450eec38eb32b50a8b29521bbd8
P356
10.1136/JMEDGENET-2014-102964
http://www.w3.org/2001/XMLSchema#string
P356
JMEDGENET-2014-102964