Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP592130.RAmQbbERK6bSf-2Bmhp-B74TTij9BdJ3GQaOY6sl972Nc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP592130.RAmQbbERK6bSf-2Bmhp-B74TTij9BdJ3GQaOY6sl972Nc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP592130.RAmQbbERK6bSf-2Bmhp-B74TTij9BdJ3GQaOY6sl972Nc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP592130.RAmQbbERK6bSf-2Bmhp-B74TTij9BdJ3GQaOY6sl972Nc130_provenance.
- NP592130.RAmQbbERK6bSf-2Bmhp-B74TTij9BdJ3GQaOY6sl972Nc130_assertion description "[Defects in NADH:ubiquinone oxidoreductase, the complex I of the mitochondrial respiratory chain represents the most frequent cause of mitochondrial diseases and is associated with a wide clinical spectrum varying from severe lactic acidosis in infants to muscle weakness in adults.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP592130.RAmQbbERK6bSf-2Bmhp-B74TTij9BdJ3GQaOY6sl972Nc130_provenance.
- NP592130.RAmQbbERK6bSf-2Bmhp-B74TTij9BdJ3GQaOY6sl972Nc130_assertion evidence source_evidence_literature NP592130.RAmQbbERK6bSf-2Bmhp-B74TTij9BdJ3GQaOY6sl972Nc130_provenance.
- NP592130.RAmQbbERK6bSf-2Bmhp-B74TTij9BdJ3GQaOY6sl972Nc130_assertion SIO_000772 17275378 NP592130.RAmQbbERK6bSf-2Bmhp-B74TTij9BdJ3GQaOY6sl972Nc130_provenance.
- NP592130.RAmQbbERK6bSf-2Bmhp-B74TTij9BdJ3GQaOY6sl972Nc130_assertion wasDerivedFrom befree-2016 NP592130.RAmQbbERK6bSf-2Bmhp-B74TTij9BdJ3GQaOY6sl972Nc130_provenance.
- NP592130.RAmQbbERK6bSf-2Bmhp-B74TTij9BdJ3GQaOY6sl972Nc130_assertion wasGeneratedBy ECO_0000203 NP592130.RAmQbbERK6bSf-2Bmhp-B74TTij9BdJ3GQaOY6sl972Nc130_provenance.
- befree-2016 importedOn "2016-02-19" NP592130.RAmQbbERK6bSf-2Bmhp-B74TTij9BdJ3GQaOY6sl972Nc130_provenance.