Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1104872.RA1XazzLvghDwO7yY9ky9n4erFo89R9d9vDzWLpPe0fVU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1104872.RA1XazzLvghDwO7yY9ky9n4erFo89R9d9vDzWLpPe0fVU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1104872.RA1XazzLvghDwO7yY9ky9n4erFo89R9d9vDzWLpPe0fVU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1104872.RA1XazzLvghDwO7yY9ky9n4erFo89R9d9vDzWLpPe0fVU130_provenance.
- befree-2016 importedOn "2016-02-19" NP1104872.RA1XazzLvghDwO7yY9ky9n4erFo89R9d9vDzWLpPe0fVU130_provenance.
- NP1104872.RA1XazzLvghDwO7yY9ky9n4erFo89R9d9vDzWLpPe0fVU130_assertion wasGeneratedBy ECO_0000203 NP1104872.RA1XazzLvghDwO7yY9ky9n4erFo89R9d9vDzWLpPe0fVU130_provenance.
- NP1104872.RA1XazzLvghDwO7yY9ky9n4erFo89R9d9vDzWLpPe0fVU130_assertion wasDerivedFrom befree-2016 NP1104872.RA1XazzLvghDwO7yY9ky9n4erFo89R9d9vDzWLpPe0fVU130_provenance.
- NP1104872.RA1XazzLvghDwO7yY9ky9n4erFo89R9d9vDzWLpPe0fVU130_assertion SIO_000772 23973714 NP1104872.RA1XazzLvghDwO7yY9ky9n4erFo89R9d9vDzWLpPe0fVU130_provenance.
- NP1104872.RA1XazzLvghDwO7yY9ky9n4erFo89R9d9vDzWLpPe0fVU130_assertion evidence source_evidence_literature NP1104872.RA1XazzLvghDwO7yY9ky9n4erFo89R9d9vDzWLpPe0fVU130_provenance.
- NP1104872.RA1XazzLvghDwO7yY9ky9n4erFo89R9d9vDzWLpPe0fVU130_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." NP1104872.RA1XazzLvghDwO7yY9ky9n4erFo89R9d9vDzWLpPe0fVU130_provenance.