Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP952050.RAN42xmQkThoR2v4I2DdNFmvesT0cG0tm4pngI7q9sS_Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP952050.RAN42xmQkThoR2v4I2DdNFmvesT0cG0tm4pngI7q9sS_Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP952050.RAN42xmQkThoR2v4I2DdNFmvesT0cG0tm4pngI7q9sS_Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP952050.RAN42xmQkThoR2v4I2DdNFmvesT0cG0tm4pngI7q9sS_Q130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP952050.RAN42xmQkThoR2v4I2DdNFmvesT0cG0tm4pngI7q9sS_Q130_provenance.