Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP539776.RA9TFhUIMF5Lmaur-lQKtdJ8mp5C_XtNr8lk1F5Y00KmY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP539776.RA9TFhUIMF5Lmaur-lQKtdJ8mp5C_XtNr8lk1F5Y00KmY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP539776.RA9TFhUIMF5Lmaur-lQKtdJ8mp5C_XtNr8lk1F5Y00KmY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP539776.RA9TFhUIMF5Lmaur-lQKtdJ8mp5C_XtNr8lk1F5Y00KmY130_provenance.
- NP539776.RA9TFhUIMF5Lmaur-lQKtdJ8mp5C_XtNr8lk1F5Y00KmY130_assertion description "[Spinocerebellar ataxia type 6 (SCA6) was recently identified as a form of autosomal dominant spinocerebellar ataxia associated with a small CAG repeat expansion of the gene encoding an alpha 1 A-voltage-dependent calcium channel gene subunit on chromosome 19p13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP539776.RA9TFhUIMF5Lmaur-lQKtdJ8mp5C_XtNr8lk1F5Y00KmY130_provenance.
- NP539776.RA9TFhUIMF5Lmaur-lQKtdJ8mp5C_XtNr8lk1F5Y00KmY130_assertion evidence source_evidence_literature NP539776.RA9TFhUIMF5Lmaur-lQKtdJ8mp5C_XtNr8lk1F5Y00KmY130_provenance.
- NP539776.RA9TFhUIMF5Lmaur-lQKtdJ8mp5C_XtNr8lk1F5Y00KmY130_assertion SIO_000772 10985694 NP539776.RA9TFhUIMF5Lmaur-lQKtdJ8mp5C_XtNr8lk1F5Y00KmY130_provenance.
- NP539776.RA9TFhUIMF5Lmaur-lQKtdJ8mp5C_XtNr8lk1F5Y00KmY130_assertion wasDerivedFrom befree-20140225 NP539776.RA9TFhUIMF5Lmaur-lQKtdJ8mp5C_XtNr8lk1F5Y00KmY130_provenance.
- NP539776.RA9TFhUIMF5Lmaur-lQKtdJ8mp5C_XtNr8lk1F5Y00KmY130_assertion wasGeneratedBy ECO_0000203 NP539776.RA9TFhUIMF5Lmaur-lQKtdJ8mp5C_XtNr8lk1F5Y00KmY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP539776.RA9TFhUIMF5Lmaur-lQKtdJ8mp5C_XtNr8lk1F5Y00KmY130_provenance.