Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1038639.RADn8JH42cg1JC4kayyK8D-agKczUR-LlBBthmTQhPCLA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1038639.RADn8JH42cg1JC4kayyK8D-agKczUR-LlBBthmTQhPCLA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1038639.RADn8JH42cg1JC4kayyK8D-agKczUR-LlBBthmTQhPCLA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1038639.RADn8JH42cg1JC4kayyK8D-agKczUR-LlBBthmTQhPCLA130_provenance.
- NP1038639.RADn8JH42cg1JC4kayyK8D-agKczUR-LlBBthmTQhPCLA130_assertion description "[Nicotinamide adenine dinucleotide (NADH):ubiquinone oxidoreductase (complex I) enzyme deficiencies account for a significant proportion of mitochondrial disorders, including LS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1038639.RADn8JH42cg1JC4kayyK8D-agKczUR-LlBBthmTQhPCLA130_provenance.
- NP1038639.RADn8JH42cg1JC4kayyK8D-agKczUR-LlBBthmTQhPCLA130_assertion evidence source_evidence_literature NP1038639.RADn8JH42cg1JC4kayyK8D-agKczUR-LlBBthmTQhPCLA130_provenance.
- NP1038639.RADn8JH42cg1JC4kayyK8D-agKczUR-LlBBthmTQhPCLA130_assertion SIO_000772 23266820 NP1038639.RADn8JH42cg1JC4kayyK8D-agKczUR-LlBBthmTQhPCLA130_provenance.
- NP1038639.RADn8JH42cg1JC4kayyK8D-agKczUR-LlBBthmTQhPCLA130_assertion wasDerivedFrom befree-2016 NP1038639.RADn8JH42cg1JC4kayyK8D-agKczUR-LlBBthmTQhPCLA130_provenance.
- NP1038639.RADn8JH42cg1JC4kayyK8D-agKczUR-LlBBthmTQhPCLA130_assertion wasGeneratedBy ECO_0000203 NP1038639.RADn8JH42cg1JC4kayyK8D-agKczUR-LlBBthmTQhPCLA130_provenance.
- befree-2016 importedOn "2016-02-19" NP1038639.RADn8JH42cg1JC4kayyK8D-agKczUR-LlBBthmTQhPCLA130_provenance.