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- source_evidence_literature type ECO_0000212 NP1038640.RA2HZfND5SxpYf_rLHaPgURfLnk9IYlG-xEKqLBP0wD0U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1038640.RA2HZfND5SxpYf_rLHaPgURfLnk9IYlG-xEKqLBP0wD0U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1038640.RA2HZfND5SxpYf_rLHaPgURfLnk9IYlG-xEKqLBP0wD0U130_provenance.
- NP1038640.RA2HZfND5SxpYf_rLHaPgURfLnk9IYlG-xEKqLBP0wD0U130_assertion description "[Leigh syndrome associated with mitochondrial complex I deficiency due to novel mutations In NDUFV1 and NDUFS2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1038640.RA2HZfND5SxpYf_rLHaPgURfLnk9IYlG-xEKqLBP0wD0U130_provenance.
- NP1038640.RA2HZfND5SxpYf_rLHaPgURfLnk9IYlG-xEKqLBP0wD0U130_assertion evidence source_evidence_literature NP1038640.RA2HZfND5SxpYf_rLHaPgURfLnk9IYlG-xEKqLBP0wD0U130_provenance.
- NP1038640.RA2HZfND5SxpYf_rLHaPgURfLnk9IYlG-xEKqLBP0wD0U130_assertion SIO_000772 23266820 NP1038640.RA2HZfND5SxpYf_rLHaPgURfLnk9IYlG-xEKqLBP0wD0U130_provenance.
- NP1038640.RA2HZfND5SxpYf_rLHaPgURfLnk9IYlG-xEKqLBP0wD0U130_assertion wasDerivedFrom befree-2016 NP1038640.RA2HZfND5SxpYf_rLHaPgURfLnk9IYlG-xEKqLBP0wD0U130_provenance.
- NP1038640.RA2HZfND5SxpYf_rLHaPgURfLnk9IYlG-xEKqLBP0wD0U130_assertion wasGeneratedBy ECO_0000203 NP1038640.RA2HZfND5SxpYf_rLHaPgURfLnk9IYlG-xEKqLBP0wD0U130_provenance.
- befree-2016 importedOn "2016-02-19" NP1038640.RA2HZfND5SxpYf_rLHaPgURfLnk9IYlG-xEKqLBP0wD0U130_provenance.