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Q51158820-1600F54B-10A0-4755-AC5D-A0BE11D8DFB8
Q51158820-1600F54B-10A0-4755-AC5D-A0BE11D8DFB8
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51158820-1600F54B-10A0-4755-AC5D-A0BE11D8DFB8
Filamin B Loss-of-Function Mutation in Dimerization Domain Causes Autosomal-Recessive Spondylocarpotarsal Synostosis Syndrome with Rib Anomalies.
P2860
Q51158820-1600F54B-10A0-4755-AC5D-A0BE11D8DFB8
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51158820-1600F54B-10A0-4755-AC5D-A0BE11D8DFB8
rank
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type
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Statement
wasDerivedFrom
33180124bff4e3ca3d54bcb0c98fdfbfea34aa9c
P2860
HomSI: a homozygous stretch identifier from next-generation sequencing data.