Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP584231.RAAatHtW1jk5OcDbBZnXEN0ZqFStx7KPaRlhEVpF8802g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP584231.RAAatHtW1jk5OcDbBZnXEN0ZqFStx7KPaRlhEVpF8802g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP584231.RAAatHtW1jk5OcDbBZnXEN0ZqFStx7KPaRlhEVpF8802g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP584231.RAAatHtW1jk5OcDbBZnXEN0ZqFStx7KPaRlhEVpF8802g130_provenance.
- NP584231.RAAatHtW1jk5OcDbBZnXEN0ZqFStx7KPaRlhEVpF8802g130_assertion description "[R162W mutation of keratin 9 in a family with autosomal dominant palmoplantar keratoderma with unique histologic features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP584231.RAAatHtW1jk5OcDbBZnXEN0ZqFStx7KPaRlhEVpF8802g130_provenance.
- NP584231.RAAatHtW1jk5OcDbBZnXEN0ZqFStx7KPaRlhEVpF8802g130_assertion evidence source_evidence_literature NP584231.RAAatHtW1jk5OcDbBZnXEN0ZqFStx7KPaRlhEVpF8802g130_provenance.
- NP584231.RAAatHtW1jk5OcDbBZnXEN0ZqFStx7KPaRlhEVpF8802g130_assertion SIO_000772 10536990 NP584231.RAAatHtW1jk5OcDbBZnXEN0ZqFStx7KPaRlhEVpF8802g130_provenance.
- NP584231.RAAatHtW1jk5OcDbBZnXEN0ZqFStx7KPaRlhEVpF8802g130_assertion wasDerivedFrom befree-20140225 NP584231.RAAatHtW1jk5OcDbBZnXEN0ZqFStx7KPaRlhEVpF8802g130_provenance.
- NP584231.RAAatHtW1jk5OcDbBZnXEN0ZqFStx7KPaRlhEVpF8802g130_assertion wasGeneratedBy ECO_0000203 NP584231.RAAatHtW1jk5OcDbBZnXEN0ZqFStx7KPaRlhEVpF8802g130_provenance.
- befree-20140225 importedOn "2014-02-25" NP584231.RAAatHtW1jk5OcDbBZnXEN0ZqFStx7KPaRlhEVpF8802g130_provenance.