Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP534988.RAF1j22bi1eIh6z-ihq_IKZRrEcgXBt4mB9uiHGt9gQwg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP534988.RAF1j22bi1eIh6z-ihq_IKZRrEcgXBt4mB9uiHGt9gQwg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP534988.RAF1j22bi1eIh6z-ihq_IKZRrEcgXBt4mB9uiHGt9gQwg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP534988.RAF1j22bi1eIh6z-ihq_IKZRrEcgXBt4mB9uiHGt9gQwg130_provenance.
- NP534988.RAF1j22bi1eIh6z-ihq_IKZRrEcgXBt4mB9uiHGt9gQwg130_assertion wasGeneratedBy ECO_0000203 NP534988.RAF1j22bi1eIh6z-ihq_IKZRrEcgXBt4mB9uiHGt9gQwg130_provenance.
- NP534988.RAF1j22bi1eIh6z-ihq_IKZRrEcgXBt4mB9uiHGt9gQwg130_assertion wasDerivedFrom befree-20140225 NP534988.RAF1j22bi1eIh6z-ihq_IKZRrEcgXBt4mB9uiHGt9gQwg130_provenance.
- NP534988.RAF1j22bi1eIh6z-ihq_IKZRrEcgXBt4mB9uiHGt9gQwg130_assertion SIO_000772 16200211 NP534988.RAF1j22bi1eIh6z-ihq_IKZRrEcgXBt4mB9uiHGt9gQwg130_provenance.
- NP534988.RAF1j22bi1eIh6z-ihq_IKZRrEcgXBt4mB9uiHGt9gQwg130_assertion evidence source_evidence_literature NP534988.RAF1j22bi1eIh6z-ihq_IKZRrEcgXBt4mB9uiHGt9gQwg130_provenance.
- NP534988.RAF1j22bi1eIh6z-ihq_IKZRrEcgXBt4mB9uiHGt9gQwg130_assertion description "[NADH:ubiquinone oxidoreductase (complex I) deficiency is a common cause of mitochondrial oxidative phosphorylation disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP534988.RAF1j22bi1eIh6z-ihq_IKZRrEcgXBt4mB9uiHGt9gQwg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP534988.RAF1j22bi1eIh6z-ihq_IKZRrEcgXBt4mB9uiHGt9gQwg130_provenance.