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Q51158820-C5A9FCE1-88E5-4D30-9B0E-AD7B687DABCB
Q51158820-C5A9FCE1-88E5-4D30-9B0E-AD7B687DABCB
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51158820-C5A9FCE1-88E5-4D30-9B0E-AD7B687DABCB
Filamin B Loss-of-Function Mutation in Dimerization Domain Causes Autosomal-Recessive Spondylocarpotarsal Synostosis Syndrome with Rib Anomalies.
P2093
Q51158820-C5A9FCE1-88E5-4D30-9B0E-AD7B687DABCB
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51158820-C5A9FCE1-88E5-4D30-9B0E-AD7B687DABCB
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
2959da6c0cdb478c3ea5c9efa051ad41573efacb
P1545
3
http://www.w3.org/2001/XMLSchema#string
P2093
Weng Siong H'ng
http://www.w3.org/2001/XMLSchema#string