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Q41928481-40C4C995-FED6-4076-9E77-0BB0A2ED7BA5
Q41928481-40C4C995-FED6-4076-9E77-0BB0A2ED7BA5
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41928481-40C4C995-FED6-4076-9E77-0BB0A2ED7BA5
A novel syndrome of Klippel-Feil anomaly, myopathy, and characteristic facies is linked to a null mutation in MYO18B.
P1476
Q41928481-40C4C995-FED6-4076-9E77-0BB0A2ED7BA5
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41928481-40C4C995-FED6-4076-9E77-0BB0A2ED7BA5
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
0cce053421955450eec38eb32b50a8b29521bbd8
P1476
A novel syndrome of Klippel-Fe
......
d to a null mutation in MYO18B
@en