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- source_evidence_literature type ECO_0000212 NP472616.RAdOvib-YP31dYbtjEje_G94pOsyuvU5cW3bMm5A-pFOg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP472616.RAdOvib-YP31dYbtjEje_G94pOsyuvU5cW3bMm5A-pFOg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP472616.RAdOvib-YP31dYbtjEje_G94pOsyuvU5cW3bMm5A-pFOg130_provenance.
- NP472616.RAdOvib-YP31dYbtjEje_G94pOsyuvU5cW3bMm5A-pFOg130_assertion description "[Three patients with AOA1 were identified in an APTX mutation screening on 28 Southern Italian patients with progressive ataxia and peripheral neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP472616.RAdOvib-YP31dYbtjEje_G94pOsyuvU5cW3bMm5A-pFOg130_provenance.
- NP472616.RAdOvib-YP31dYbtjEje_G94pOsyuvU5cW3bMm5A-pFOg130_assertion evidence source_evidence_literature NP472616.RAdOvib-YP31dYbtjEje_G94pOsyuvU5cW3bMm5A-pFOg130_provenance.
- NP472616.RAdOvib-YP31dYbtjEje_G94pOsyuvU5cW3bMm5A-pFOg130_assertion SIO_000772 15596775 NP472616.RAdOvib-YP31dYbtjEje_G94pOsyuvU5cW3bMm5A-pFOg130_provenance.
- NP472616.RAdOvib-YP31dYbtjEje_G94pOsyuvU5cW3bMm5A-pFOg130_assertion wasDerivedFrom befree-2016 NP472616.RAdOvib-YP31dYbtjEje_G94pOsyuvU5cW3bMm5A-pFOg130_provenance.
- NP472616.RAdOvib-YP31dYbtjEje_G94pOsyuvU5cW3bMm5A-pFOg130_assertion wasGeneratedBy ECO_0000203 NP472616.RAdOvib-YP31dYbtjEje_G94pOsyuvU5cW3bMm5A-pFOg130_provenance.
- befree-2016 importedOn "2016-02-19" NP472616.RAdOvib-YP31dYbtjEje_G94pOsyuvU5cW3bMm5A-pFOg130_provenance.