Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP824564.RAqqQGqgQQC5UyoDRJloT8WmQGRvKY4Tpiuj38vtM50cY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP824564.RAqqQGqgQQC5UyoDRJloT8WmQGRvKY4Tpiuj38vtM50cY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP824564.RAqqQGqgQQC5UyoDRJloT8WmQGRvKY4Tpiuj38vtM50cY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP824564.RAqqQGqgQQC5UyoDRJloT8WmQGRvKY4Tpiuj38vtM50cY130_provenance.
- NP824564.RAqqQGqgQQC5UyoDRJloT8WmQGRvKY4Tpiuj38vtM50cY130_assertion description "[Mutations found in this gene (NADH dehydrogenase iron-sulphur protein 3), coding for the seventh and last subunit of complex I core, were shown to cause late onset Leigh syndrome, optic atrophy, and complex I deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP824564.RAqqQGqgQQC5UyoDRJloT8WmQGRvKY4Tpiuj38vtM50cY130_provenance.
- NP824564.RAqqQGqgQQC5UyoDRJloT8WmQGRvKY4Tpiuj38vtM50cY130_assertion evidence source_evidence_literature NP824564.RAqqQGqgQQC5UyoDRJloT8WmQGRvKY4Tpiuj38vtM50cY130_provenance.
- NP824564.RAqqQGqgQQC5UyoDRJloT8WmQGRvKY4Tpiuj38vtM50cY130_assertion SIO_000772 14729820 NP824564.RAqqQGqgQQC5UyoDRJloT8WmQGRvKY4Tpiuj38vtM50cY130_provenance.
- NP824564.RAqqQGqgQQC5UyoDRJloT8WmQGRvKY4Tpiuj38vtM50cY130_assertion wasDerivedFrom befree-20140225 NP824564.RAqqQGqgQQC5UyoDRJloT8WmQGRvKY4Tpiuj38vtM50cY130_provenance.
- NP824564.RAqqQGqgQQC5UyoDRJloT8WmQGRvKY4Tpiuj38vtM50cY130_assertion wasGeneratedBy ECO_0000203 NP824564.RAqqQGqgQQC5UyoDRJloT8WmQGRvKY4Tpiuj38vtM50cY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP824564.RAqqQGqgQQC5UyoDRJloT8WmQGRvKY4Tpiuj38vtM50cY130_provenance.