Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP304456.RA3l2H5YpauTF5A4Ekzds0EYqRSwgF9czw9rZSrebpkR0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP304456.RA3l2H5YpauTF5A4Ekzds0EYqRSwgF9czw9rZSrebpkR0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP304456.RA3l2H5YpauTF5A4Ekzds0EYqRSwgF9czw9rZSrebpkR0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP304456.RA3l2H5YpauTF5A4Ekzds0EYqRSwgF9czw9rZSrebpkR0130_provenance.
- NP304456.RA3l2H5YpauTF5A4Ekzds0EYqRSwgF9czw9rZSrebpkR0130_assertion description "[Cycle sequencing of amplified NDUFS8 cDNA of 20 patients with isolated enzymatic complex I deficiency revealed two compound heterozygous transitions in a patient with neuropathologically proven Leigh syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP304456.RA3l2H5YpauTF5A4Ekzds0EYqRSwgF9czw9rZSrebpkR0130_provenance.
- NP304456.RA3l2H5YpauTF5A4Ekzds0EYqRSwgF9czw9rZSrebpkR0130_assertion evidence source_evidence_literature NP304456.RA3l2H5YpauTF5A4Ekzds0EYqRSwgF9czw9rZSrebpkR0130_provenance.
- NP304456.RA3l2H5YpauTF5A4Ekzds0EYqRSwgF9czw9rZSrebpkR0130_assertion SIO_000772 9837812 NP304456.RA3l2H5YpauTF5A4Ekzds0EYqRSwgF9czw9rZSrebpkR0130_provenance.
- NP304456.RA3l2H5YpauTF5A4Ekzds0EYqRSwgF9czw9rZSrebpkR0130_assertion wasDerivedFrom befree-20140225 NP304456.RA3l2H5YpauTF5A4Ekzds0EYqRSwgF9czw9rZSrebpkR0130_provenance.
- NP304456.RA3l2H5YpauTF5A4Ekzds0EYqRSwgF9czw9rZSrebpkR0130_assertion wasGeneratedBy ECO_0000203 NP304456.RA3l2H5YpauTF5A4Ekzds0EYqRSwgF9czw9rZSrebpkR0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP304456.RA3l2H5YpauTF5A4Ekzds0EYqRSwgF9czw9rZSrebpkR0130_provenance.