Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP576677.RA_wW4vKvLbyLWneISSlZP4vHH7Q-QAU86lKu9Y4jLGTs130_assertion> ?p ?o ?g. }
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- NP576677.RA_wW4vKvLbyLWneISSlZP4vHH7Q-QAU86lKu9Y4jLGTs130_assertion type Assertion NP576677.RA_wW4vKvLbyLWneISSlZP4vHH7Q-QAU86lKu9Y4jLGTs130_head.
- 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.