Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP476100.RAuAftSAkFIwE-NsEZLLdcO8SgCM4uqJ15yCHxETtAaj0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP476100.RAuAftSAkFIwE-NsEZLLdcO8SgCM4uqJ15yCHxETtAaj0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP476100.RAuAftSAkFIwE-NsEZLLdcO8SgCM4uqJ15yCHxETtAaj0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP476100.RAuAftSAkFIwE-NsEZLLdcO8SgCM4uqJ15yCHxETtAaj0130_provenance.
- NP476100.RAuAftSAkFIwE-NsEZLLdcO8SgCM4uqJ15yCHxETtAaj0130_assertion description "[The ND1 subunit gene of the mitochondrial NADH-ubiquinone oxidoreductase (complex I) is a hot spot for mutations causing Leber hereditary optic neuropathy and several mutations causing the mitochondrial encephalopathy, lactic acidosis and stroke-like episodes syndrome (MELAS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP476100.RAuAftSAkFIwE-NsEZLLdcO8SgCM4uqJ15yCHxETtAaj0130_provenance.
- NP476100.RAuAftSAkFIwE-NsEZLLdcO8SgCM4uqJ15yCHxETtAaj0130_assertion evidence source_evidence_literature NP476100.RAuAftSAkFIwE-NsEZLLdcO8SgCM4uqJ15yCHxETtAaj0130_provenance.
- NP476100.RAuAftSAkFIwE-NsEZLLdcO8SgCM4uqJ15yCHxETtAaj0130_assertion SIO_000772 16849371 NP476100.RAuAftSAkFIwE-NsEZLLdcO8SgCM4uqJ15yCHxETtAaj0130_provenance.
- NP476100.RAuAftSAkFIwE-NsEZLLdcO8SgCM4uqJ15yCHxETtAaj0130_assertion wasDerivedFrom befree-20140225 NP476100.RAuAftSAkFIwE-NsEZLLdcO8SgCM4uqJ15yCHxETtAaj0130_provenance.
- NP476100.RAuAftSAkFIwE-NsEZLLdcO8SgCM4uqJ15yCHxETtAaj0130_assertion wasGeneratedBy ECO_0000203 NP476100.RAuAftSAkFIwE-NsEZLLdcO8SgCM4uqJ15yCHxETtAaj0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP476100.RAuAftSAkFIwE-NsEZLLdcO8SgCM4uqJ15yCHxETtAaj0130_provenance.