Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP836872.RAJj4itIGDFBVsyII6SBH-WI9lJAJHrnyH4v1F2IzuY_s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP836872.RAJj4itIGDFBVsyII6SBH-WI9lJAJHrnyH4v1F2IzuY_s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP836872.RAJj4itIGDFBVsyII6SBH-WI9lJAJHrnyH4v1F2IzuY_s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP836872.RAJj4itIGDFBVsyII6SBH-WI9lJAJHrnyH4v1F2IzuY_s130_provenance.
- NP836872.RAJj4itIGDFBVsyII6SBH-WI9lJAJHrnyH4v1F2IzuY_s130_assertion description "[LRPPRC mutations cause a phenotypically distinct form of Leigh syndrome with cytochrome c oxidase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP836872.RAJj4itIGDFBVsyII6SBH-WI9lJAJHrnyH4v1F2IzuY_s130_provenance.
- NP836872.RAJj4itIGDFBVsyII6SBH-WI9lJAJHrnyH4v1F2IzuY_s130_assertion evidence source_evidence_literature NP836872.RAJj4itIGDFBVsyII6SBH-WI9lJAJHrnyH4v1F2IzuY_s130_provenance.
- NP836872.RAJj4itIGDFBVsyII6SBH-WI9lJAJHrnyH4v1F2IzuY_s130_assertion SIO_000772 21266382 NP836872.RAJj4itIGDFBVsyII6SBH-WI9lJAJHrnyH4v1F2IzuY_s130_provenance.
- NP836872.RAJj4itIGDFBVsyII6SBH-WI9lJAJHrnyH4v1F2IzuY_s130_assertion wasDerivedFrom befree-20150227 NP836872.RAJj4itIGDFBVsyII6SBH-WI9lJAJHrnyH4v1F2IzuY_s130_provenance.
- NP836872.RAJj4itIGDFBVsyII6SBH-WI9lJAJHrnyH4v1F2IzuY_s130_assertion wasGeneratedBy ECO_0000203 NP836872.RAJj4itIGDFBVsyII6SBH-WI9lJAJHrnyH4v1F2IzuY_s130_provenance.
- befree-20150227 importedOn "2015-02-27" NP836872.RAJj4itIGDFBVsyII6SBH-WI9lJAJHrnyH4v1F2IzuY_s130_provenance.