Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1011086.RASsDSGdcEN6FX94tixbXYXU-AlqoWVpWzRnPptDFgZiY130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1011086.RASsDSGdcEN6FX94tixbXYXU-AlqoWVpWzRnPptDFgZiY130_assertion type Assertion NP1011086.RASsDSGdcEN6FX94tixbXYXU-AlqoWVpWzRnPptDFgZiY130_head.
- NP1011086.RASsDSGdcEN6FX94tixbXYXU-AlqoWVpWzRnPptDFgZiY130_assertion wasGeneratedBy ECO_0000203 NP1011086.RASsDSGdcEN6FX94tixbXYXU-AlqoWVpWzRnPptDFgZiY130_provenance.
- NP1011086.RASsDSGdcEN6FX94tixbXYXU-AlqoWVpWzRnPptDFgZiY130_assertion wasDerivedFrom befree-20150227 NP1011086.RASsDSGdcEN6FX94tixbXYXU-AlqoWVpWzRnPptDFgZiY130_provenance.
- NP1011086.RASsDSGdcEN6FX94tixbXYXU-AlqoWVpWzRnPptDFgZiY130_assertion SIO_000772 23973714 NP1011086.RASsDSGdcEN6FX94tixbXYXU-AlqoWVpWzRnPptDFgZiY130_provenance.
- NP1011086.RASsDSGdcEN6FX94tixbXYXU-AlqoWVpWzRnPptDFgZiY130_assertion evidence source_evidence_literature NP1011086.RASsDSGdcEN6FX94tixbXYXU-AlqoWVpWzRnPptDFgZiY130_provenance.
- NP1011086.RASsDSGdcEN6FX94tixbXYXU-AlqoWVpWzRnPptDFgZiY130_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." NP1011086.RASsDSGdcEN6FX94tixbXYXU-AlqoWVpWzRnPptDFgZiY130_provenance.