Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP576677.RA_wW4vKvLbyLWneISSlZP4vHH7Q-QAU86lKu9Y4jLGTs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP576677.RA_wW4vKvLbyLWneISSlZP4vHH7Q-QAU86lKu9Y4jLGTs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP576677.RA_wW4vKvLbyLWneISSlZP4vHH7Q-QAU86lKu9Y4jLGTs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP576677.RA_wW4vKvLbyLWneISSlZP4vHH7Q-QAU86lKu9Y4jLGTs130_provenance.
- NP576677.RA_wW4vKvLbyLWneISSlZP4vHH7Q-QAU86lKu9Y4jLGTs130_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." NP576677.RA_wW4vKvLbyLWneISSlZP4vHH7Q-QAU86lKu9Y4jLGTs130_provenance.
- NP576677.RA_wW4vKvLbyLWneISSlZP4vHH7Q-QAU86lKu9Y4jLGTs130_assertion evidence source_evidence_literature NP576677.RA_wW4vKvLbyLWneISSlZP4vHH7Q-QAU86lKu9Y4jLGTs130_provenance.
- NP576677.RA_wW4vKvLbyLWneISSlZP4vHH7Q-QAU86lKu9Y4jLGTs130_assertion SIO_000772 7654063 NP576677.RA_wW4vKvLbyLWneISSlZP4vHH7Q-QAU86lKu9Y4jLGTs130_provenance.
- NP576677.RA_wW4vKvLbyLWneISSlZP4vHH7Q-QAU86lKu9Y4jLGTs130_assertion wasDerivedFrom befree-20150227 NP576677.RA_wW4vKvLbyLWneISSlZP4vHH7Q-QAU86lKu9Y4jLGTs130_provenance.
- NP576677.RA_wW4vKvLbyLWneISSlZP4vHH7Q-QAU86lKu9Y4jLGTs130_assertion wasGeneratedBy ECO_0000203 NP576677.RA_wW4vKvLbyLWneISSlZP4vHH7Q-QAU86lKu9Y4jLGTs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP576677.RA_wW4vKvLbyLWneISSlZP4vHH7Q-QAU86lKu9Y4jLGTs130_provenance.