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- source_evidence_literature type ECO_0000212 NP428487.RABSll7aqkU3jZx7BlvajIBBNspZLCoxY7cNMto10C2qE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP428487.RABSll7aqkU3jZx7BlvajIBBNspZLCoxY7cNMto10C2qE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP428487.RABSll7aqkU3jZx7BlvajIBBNspZLCoxY7cNMto10C2qE130_provenance.
- NP428487.RABSll7aqkU3jZx7BlvajIBBNspZLCoxY7cNMto10C2qE130_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." NP428487.RABSll7aqkU3jZx7BlvajIBBNspZLCoxY7cNMto10C2qE130_provenance.
- NP428487.RABSll7aqkU3jZx7BlvajIBBNspZLCoxY7cNMto10C2qE130_assertion evidence source_evidence_literature NP428487.RABSll7aqkU3jZx7BlvajIBBNspZLCoxY7cNMto10C2qE130_provenance.
- NP428487.RABSll7aqkU3jZx7BlvajIBBNspZLCoxY7cNMto10C2qE130_assertion SIO_000772 14729820 NP428487.RABSll7aqkU3jZx7BlvajIBBNspZLCoxY7cNMto10C2qE130_provenance.
- NP428487.RABSll7aqkU3jZx7BlvajIBBNspZLCoxY7cNMto10C2qE130_assertion wasDerivedFrom befree-2016 NP428487.RABSll7aqkU3jZx7BlvajIBBNspZLCoxY7cNMto10C2qE130_provenance.
- NP428487.RABSll7aqkU3jZx7BlvajIBBNspZLCoxY7cNMto10C2qE130_assertion wasGeneratedBy ECO_0000203 NP428487.RABSll7aqkU3jZx7BlvajIBBNspZLCoxY7cNMto10C2qE130_provenance.
- befree-2016 importedOn "2016-02-19" NP428487.RABSll7aqkU3jZx7BlvajIBBNspZLCoxY7cNMto10C2qE130_provenance.