Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1038640.RA2HZfND5SxpYf_rLHaPgURfLnk9IYlG-xEKqLBP0wD0U130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1038640.RA2HZfND5SxpYf_rLHaPgURfLnk9IYlG-xEKqLBP0wD0U130_assertion type Assertion NP1038640.RA2HZfND5SxpYf_rLHaPgURfLnk9IYlG-xEKqLBP0wD0U130_head.
- 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.