Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1104882.RAg3UEjXxr9lkm4YLTKhcTW9M7n6voFJPgugGAvgd0HRo130_assertion> ?p ?o ?g. }
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- NP1104882.RAg3UEjXxr9lkm4YLTKhcTW9M7n6voFJPgugGAvgd0HRo130_assertion type Assertion NP1104882.RAg3UEjXxr9lkm4YLTKhcTW9M7n6voFJPgugGAvgd0HRo130_head.
- NP1104882.RAg3UEjXxr9lkm4YLTKhcTW9M7n6voFJPgugGAvgd0HRo130_assertion wasGeneratedBy ECO_0000203 NP1104882.RAg3UEjXxr9lkm4YLTKhcTW9M7n6voFJPgugGAvgd0HRo130_provenance.
- NP1104882.RAg3UEjXxr9lkm4YLTKhcTW9M7n6voFJPgugGAvgd0HRo130_assertion wasDerivedFrom befree-2016 NP1104882.RAg3UEjXxr9lkm4YLTKhcTW9M7n6voFJPgugGAvgd0HRo130_provenance.
- NP1104882.RAg3UEjXxr9lkm4YLTKhcTW9M7n6voFJPgugGAvgd0HRo130_assertion SIO_000772 23973714 NP1104882.RAg3UEjXxr9lkm4YLTKhcTW9M7n6voFJPgugGAvgd0HRo130_provenance.
- NP1104882.RAg3UEjXxr9lkm4YLTKhcTW9M7n6voFJPgugGAvgd0HRo130_assertion evidence source_evidence_literature NP1104882.RAg3UEjXxr9lkm4YLTKhcTW9M7n6voFJPgugGAvgd0HRo130_provenance.
- NP1104882.RAg3UEjXxr9lkm4YLTKhcTW9M7n6voFJPgugGAvgd0HRo130_assertion description "[Our findings that the frequency of the haplotype AAC, and AAT were significantly higher in the unaffected cases and the frequencies of haplotype GGT were significantly higher in LHON cases, indicate that it might have a role in the penetrance of this mitochondrial disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1104882.RAg3UEjXxr9lkm4YLTKhcTW9M7n6voFJPgugGAvgd0HRo130_provenance.