Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP571229.RAdzdylCDaBBGC1BtN8vjt_kGVufqDoUiPgVFUbsMvBho130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP571229.RAdzdylCDaBBGC1BtN8vjt_kGVufqDoUiPgVFUbsMvBho130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP571229.RAdzdylCDaBBGC1BtN8vjt_kGVufqDoUiPgVFUbsMvBho130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP571229.RAdzdylCDaBBGC1BtN8vjt_kGVufqDoUiPgVFUbsMvBho130_provenance.
- NP571229.RAdzdylCDaBBGC1BtN8vjt_kGVufqDoUiPgVFUbsMvBho130_assertion description "[POLG1, C10ORF2, and ANT1 mutations are uncommon in sporadic progressive external ophthalmoplegia with multiple mitochondrial DNA deletions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP571229.RAdzdylCDaBBGC1BtN8vjt_kGVufqDoUiPgVFUbsMvBho130_provenance.
- NP571229.RAdzdylCDaBBGC1BtN8vjt_kGVufqDoUiPgVFUbsMvBho130_assertion evidence source_evidence_literature NP571229.RAdzdylCDaBBGC1BtN8vjt_kGVufqDoUiPgVFUbsMvBho130_provenance.
- NP571229.RAdzdylCDaBBGC1BtN8vjt_kGVufqDoUiPgVFUbsMvBho130_assertion SIO_000772 16682683 NP571229.RAdzdylCDaBBGC1BtN8vjt_kGVufqDoUiPgVFUbsMvBho130_provenance.
- NP571229.RAdzdylCDaBBGC1BtN8vjt_kGVufqDoUiPgVFUbsMvBho130_assertion wasDerivedFrom befree-20140225 NP571229.RAdzdylCDaBBGC1BtN8vjt_kGVufqDoUiPgVFUbsMvBho130_provenance.
- NP571229.RAdzdylCDaBBGC1BtN8vjt_kGVufqDoUiPgVFUbsMvBho130_assertion wasGeneratedBy ECO_0000203 NP571229.RAdzdylCDaBBGC1BtN8vjt_kGVufqDoUiPgVFUbsMvBho130_provenance.
- befree-20140225 importedOn "2014-02-25" NP571229.RAdzdylCDaBBGC1BtN8vjt_kGVufqDoUiPgVFUbsMvBho130_provenance.