Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP199832.RA9xfD86kug-CUteZrx8aIOrttM42qeiRYl0Ij8yHu-ic130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP199832.RA9xfD86kug-CUteZrx8aIOrttM42qeiRYl0Ij8yHu-ic130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP199832.RA9xfD86kug-CUteZrx8aIOrttM42qeiRYl0Ij8yHu-ic130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP199832.RA9xfD86kug-CUteZrx8aIOrttM42qeiRYl0Ij8yHu-ic130_provenance.
- NP199832.RA9xfD86kug-CUteZrx8aIOrttM42qeiRYl0Ij8yHu-ic130_assertion description "[A patient with Leigh syndrome (LS), born to consanguineous parents, with severe complex I defect and a novel mutation in the NDUFS7 gene subunit.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199832.RA9xfD86kug-CUteZrx8aIOrttM42qeiRYl0Ij8yHu-ic130_provenance.
- NP199832.RA9xfD86kug-CUteZrx8aIOrttM42qeiRYl0Ij8yHu-ic130_assertion evidence source_evidence_literature NP199832.RA9xfD86kug-CUteZrx8aIOrttM42qeiRYl0Ij8yHu-ic130_provenance.
- NP199832.RA9xfD86kug-CUteZrx8aIOrttM42qeiRYl0Ij8yHu-ic130_assertion SIO_000772 17275378 NP199832.RA9xfD86kug-CUteZrx8aIOrttM42qeiRYl0Ij8yHu-ic130_provenance.
- NP199832.RA9xfD86kug-CUteZrx8aIOrttM42qeiRYl0Ij8yHu-ic130_assertion wasDerivedFrom lhgdn-20090331 NP199832.RA9xfD86kug-CUteZrx8aIOrttM42qeiRYl0Ij8yHu-ic130_provenance.
- NP199832.RA9xfD86kug-CUteZrx8aIOrttM42qeiRYl0Ij8yHu-ic130_assertion wasGeneratedBy ECO_0000203 NP199832.RA9xfD86kug-CUteZrx8aIOrttM42qeiRYl0Ij8yHu-ic130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP199832.RA9xfD86kug-CUteZrx8aIOrttM42qeiRYl0Ij8yHu-ic130_provenance.