Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP952050.RAN42xmQkThoR2v4I2DdNFmvesT0cG0tm4pngI7q9sS_Q130_assertion> ?p ?o ?g. }
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- NP952050.RAN42xmQkThoR2v4I2DdNFmvesT0cG0tm4pngI7q9sS_Q130_assertion type Assertion NP952050.RAN42xmQkThoR2v4I2DdNFmvesT0cG0tm4pngI7q9sS_Q130_head.
- NP952050.RAN42xmQkThoR2v4I2DdNFmvesT0cG0tm4pngI7q9sS_Q130_assertion description "[Individuals who came from two families and met the diagnostic criteria for WMS were each found to have a different homozygous missense mutation in ADAMTS10.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP952050.RAN42xmQkThoR2v4I2DdNFmvesT0cG0tm4pngI7q9sS_Q130_provenance.
- NP952050.RAN42xmQkThoR2v4I2DdNFmvesT0cG0tm4pngI7q9sS_Q130_assertion evidence source_evidence_literature NP952050.RAN42xmQkThoR2v4I2DdNFmvesT0cG0tm4pngI7q9sS_Q130_provenance.
- NP952050.RAN42xmQkThoR2v4I2DdNFmvesT0cG0tm4pngI7q9sS_Q130_assertion SIO_000772 19836009 NP952050.RAN42xmQkThoR2v4I2DdNFmvesT0cG0tm4pngI7q9sS_Q130_provenance.
- NP952050.RAN42xmQkThoR2v4I2DdNFmvesT0cG0tm4pngI7q9sS_Q130_assertion wasDerivedFrom befree-20150227 NP952050.RAN42xmQkThoR2v4I2DdNFmvesT0cG0tm4pngI7q9sS_Q130_provenance.
- NP952050.RAN42xmQkThoR2v4I2DdNFmvesT0cG0tm4pngI7q9sS_Q130_assertion wasGeneratedBy ECO_0000203 NP952050.RAN42xmQkThoR2v4I2DdNFmvesT0cG0tm4pngI7q9sS_Q130_provenance.