Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP382015.RA8tWaswIfrvdyykjXG1oD6icb6YsBNTeWGlHNveIyVFc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP382015.RA8tWaswIfrvdyykjXG1oD6icb6YsBNTeWGlHNveIyVFc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP382015.RA8tWaswIfrvdyykjXG1oD6icb6YsBNTeWGlHNveIyVFc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP382015.RA8tWaswIfrvdyykjXG1oD6icb6YsBNTeWGlHNveIyVFc130_provenance.
- NP382015.RA8tWaswIfrvdyykjXG1oD6icb6YsBNTeWGlHNveIyVFc130_assertion description "[Point mutations in the XPD gene lead either to the cancer-prone repair syndrome XP, sometimes in combination with a second repair condition; Cockayne syndrome; or the non-cancer-prone brittle-hair disorder trichothiodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP382015.RA8tWaswIfrvdyykjXG1oD6icb6YsBNTeWGlHNveIyVFc130_provenance.
- NP382015.RA8tWaswIfrvdyykjXG1oD6icb6YsBNTeWGlHNveIyVFc130_assertion evidence source_evidence_literature NP382015.RA8tWaswIfrvdyykjXG1oD6icb6YsBNTeWGlHNveIyVFc130_provenance.
- NP382015.RA8tWaswIfrvdyykjXG1oD6icb6YsBNTeWGlHNveIyVFc130_assertion SIO_000772 9426063 NP382015.RA8tWaswIfrvdyykjXG1oD6icb6YsBNTeWGlHNveIyVFc130_provenance.
- NP382015.RA8tWaswIfrvdyykjXG1oD6icb6YsBNTeWGlHNveIyVFc130_assertion wasDerivedFrom befree-20150227 NP382015.RA8tWaswIfrvdyykjXG1oD6icb6YsBNTeWGlHNveIyVFc130_provenance.
- NP382015.RA8tWaswIfrvdyykjXG1oD6icb6YsBNTeWGlHNveIyVFc130_assertion wasGeneratedBy ECO_0000203 NP382015.RA8tWaswIfrvdyykjXG1oD6icb6YsBNTeWGlHNveIyVFc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP382015.RA8tWaswIfrvdyykjXG1oD6icb6YsBNTeWGlHNveIyVFc130_provenance.