Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1316621.RArvnGOjsg8QUW2hT9XtpHV6NAajhd8yjvzRGQmXy2Irg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1316621.RArvnGOjsg8QUW2hT9XtpHV6NAajhd8yjvzRGQmXy2Irg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1316621.RArvnGOjsg8QUW2hT9XtpHV6NAajhd8yjvzRGQmXy2Irg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1316621.RArvnGOjsg8QUW2hT9XtpHV6NAajhd8yjvzRGQmXy2Irg130_provenance.
- NP1316621.RArvnGOjsg8QUW2hT9XtpHV6NAajhd8yjvzRGQmXy2Irg130_assertion description "[These results confirm the association of the MTND6*LDYT14459A mutation with Leber's hereditary optic neuropathy and/or dystonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1316621.RArvnGOjsg8QUW2hT9XtpHV6NAajhd8yjvzRGQmXy2Irg130_provenance.
- NP1316621.RArvnGOjsg8QUW2hT9XtpHV6NAajhd8yjvzRGQmXy2Irg130_assertion evidence source_evidence_literature NP1316621.RArvnGOjsg8QUW2hT9XtpHV6NAajhd8yjvzRGQmXy2Irg130_provenance.
- NP1316621.RArvnGOjsg8QUW2hT9XtpHV6NAajhd8yjvzRGQmXy2Irg130_assertion SIO_000772 7654063 NP1316621.RArvnGOjsg8QUW2hT9XtpHV6NAajhd8yjvzRGQmXy2Irg130_provenance.
- NP1316621.RArvnGOjsg8QUW2hT9XtpHV6NAajhd8yjvzRGQmXy2Irg130_assertion wasDerivedFrom befree-2016 NP1316621.RArvnGOjsg8QUW2hT9XtpHV6NAajhd8yjvzRGQmXy2Irg130_provenance.
- NP1316621.RArvnGOjsg8QUW2hT9XtpHV6NAajhd8yjvzRGQmXy2Irg130_assertion wasGeneratedBy ECO_0000203 NP1316621.RArvnGOjsg8QUW2hT9XtpHV6NAajhd8yjvzRGQmXy2Irg130_provenance.
- befree-2016 importedOn "2016-02-19" NP1316621.RArvnGOjsg8QUW2hT9XtpHV6NAajhd8yjvzRGQmXy2Irg130_provenance.