Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1005648.RAO3iCgDLyhz6_6Qff6vtQP5oeWEdjVSMWJSpCo_PdrUo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1005648.RAO3iCgDLyhz6_6Qff6vtQP5oeWEdjVSMWJSpCo_PdrUo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1005648.RAO3iCgDLyhz6_6Qff6vtQP5oeWEdjVSMWJSpCo_PdrUo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1005648.RAO3iCgDLyhz6_6Qff6vtQP5oeWEdjVSMWJSpCo_PdrUo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP1005648.RAO3iCgDLyhz6_6Qff6vtQP5oeWEdjVSMWJSpCo_PdrUo130_provenance.
- NP1005648.RAO3iCgDLyhz6_6Qff6vtQP5oeWEdjVSMWJSpCo_PdrUo130_assertion wasGeneratedBy ECO_0000203 NP1005648.RAO3iCgDLyhz6_6Qff6vtQP5oeWEdjVSMWJSpCo_PdrUo130_provenance.
- NP1005648.RAO3iCgDLyhz6_6Qff6vtQP5oeWEdjVSMWJSpCo_PdrUo130_assertion wasDerivedFrom befree-20150227 NP1005648.RAO3iCgDLyhz6_6Qff6vtQP5oeWEdjVSMWJSpCo_PdrUo130_provenance.
- NP1005648.RAO3iCgDLyhz6_6Qff6vtQP5oeWEdjVSMWJSpCo_PdrUo130_assertion SIO_000772 23973714 NP1005648.RAO3iCgDLyhz6_6Qff6vtQP5oeWEdjVSMWJSpCo_PdrUo130_provenance.
- NP1005648.RAO3iCgDLyhz6_6Qff6vtQP5oeWEdjVSMWJSpCo_PdrUo130_assertion evidence source_evidence_literature NP1005648.RAO3iCgDLyhz6_6Qff6vtQP5oeWEdjVSMWJSpCo_PdrUo130_provenance.
- NP1005648.RAO3iCgDLyhz6_6Qff6vtQP5oeWEdjVSMWJSpCo_PdrUo130_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." NP1005648.RAO3iCgDLyhz6_6Qff6vtQP5oeWEdjVSMWJSpCo_PdrUo130_provenance.