Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP824564.RAqqQGqgQQC5UyoDRJloT8WmQGRvKY4Tpiuj38vtM50cY130_assertion> ?p ?o ?g. }
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- NP824564.RAqqQGqgQQC5UyoDRJloT8WmQGRvKY4Tpiuj38vtM50cY130_assertion type Assertion NP824564.RAqqQGqgQQC5UyoDRJloT8WmQGRvKY4Tpiuj38vtM50cY130_head.
- 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.