Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP550909.RA8Hxy6pvybjMUtYIaN15x4AkivngPW8SIjm15Fn6lJsU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP550909.RA8Hxy6pvybjMUtYIaN15x4AkivngPW8SIjm15Fn6lJsU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP550909.RA8Hxy6pvybjMUtYIaN15x4AkivngPW8SIjm15Fn6lJsU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP550909.RA8Hxy6pvybjMUtYIaN15x4AkivngPW8SIjm15Fn6lJsU130_provenance.
- NP550909.RA8Hxy6pvybjMUtYIaN15x4AkivngPW8SIjm15Fn6lJsU130_assertion description "[Autosomal recessive ataxia with peripheral neuropathy and elevated AFP: novel mutations in SETX.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP550909.RA8Hxy6pvybjMUtYIaN15x4AkivngPW8SIjm15Fn6lJsU130_provenance.
- NP550909.RA8Hxy6pvybjMUtYIaN15x4AkivngPW8SIjm15Fn6lJsU130_assertion evidence source_evidence_literature NP550909.RA8Hxy6pvybjMUtYIaN15x4AkivngPW8SIjm15Fn6lJsU130_provenance.
- NP550909.RA8Hxy6pvybjMUtYIaN15x4AkivngPW8SIjm15Fn6lJsU130_assertion SIO_000772 16717225 NP550909.RA8Hxy6pvybjMUtYIaN15x4AkivngPW8SIjm15Fn6lJsU130_provenance.
- NP550909.RA8Hxy6pvybjMUtYIaN15x4AkivngPW8SIjm15Fn6lJsU130_assertion wasDerivedFrom befree-2016 NP550909.RA8Hxy6pvybjMUtYIaN15x4AkivngPW8SIjm15Fn6lJsU130_provenance.
- NP550909.RA8Hxy6pvybjMUtYIaN15x4AkivngPW8SIjm15Fn6lJsU130_assertion wasGeneratedBy ECO_0000203 NP550909.RA8Hxy6pvybjMUtYIaN15x4AkivngPW8SIjm15Fn6lJsU130_provenance.
- befree-2016 importedOn "2016-02-19" NP550909.RA8Hxy6pvybjMUtYIaN15x4AkivngPW8SIjm15Fn6lJsU130_provenance.