Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP428489.RAKYZmEX1ofmDuuJjcdKgo9OzsvhV4rht3S3ZlBbN5AMM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP428489.RAKYZmEX1ofmDuuJjcdKgo9OzsvhV4rht3S3ZlBbN5AMM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP428489.RAKYZmEX1ofmDuuJjcdKgo9OzsvhV4rht3S3ZlBbN5AMM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP428489.RAKYZmEX1ofmDuuJjcdKgo9OzsvhV4rht3S3ZlBbN5AMM130_provenance.
- NP428489.RAKYZmEX1ofmDuuJjcdKgo9OzsvhV4rht3S3ZlBbN5AMM130_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." NP428489.RAKYZmEX1ofmDuuJjcdKgo9OzsvhV4rht3S3ZlBbN5AMM130_provenance.
- NP428489.RAKYZmEX1ofmDuuJjcdKgo9OzsvhV4rht3S3ZlBbN5AMM130_assertion evidence source_evidence_literature NP428489.RAKYZmEX1ofmDuuJjcdKgo9OzsvhV4rht3S3ZlBbN5AMM130_provenance.
- NP428489.RAKYZmEX1ofmDuuJjcdKgo9OzsvhV4rht3S3ZlBbN5AMM130_assertion SIO_000772 14729820 NP428489.RAKYZmEX1ofmDuuJjcdKgo9OzsvhV4rht3S3ZlBbN5AMM130_provenance.
- NP428489.RAKYZmEX1ofmDuuJjcdKgo9OzsvhV4rht3S3ZlBbN5AMM130_assertion wasDerivedFrom befree-2016 NP428489.RAKYZmEX1ofmDuuJjcdKgo9OzsvhV4rht3S3ZlBbN5AMM130_provenance.
- NP428489.RAKYZmEX1ofmDuuJjcdKgo9OzsvhV4rht3S3ZlBbN5AMM130_assertion wasGeneratedBy ECO_0000203 NP428489.RAKYZmEX1ofmDuuJjcdKgo9OzsvhV4rht3S3ZlBbN5AMM130_provenance.
- befree-2016 importedOn "2016-02-19" NP428489.RAKYZmEX1ofmDuuJjcdKgo9OzsvhV4rht3S3ZlBbN5AMM130_provenance.