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- source_evidence_literature type ECO_0000212 NP1246897.RAnkx872aJV5uZUXjRy_q0J8qFzCunug_GqRpBgPtonCA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1246897.RAnkx872aJV5uZUXjRy_q0J8qFzCunug_GqRpBgPtonCA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1246897.RAnkx872aJV5uZUXjRy_q0J8qFzCunug_GqRpBgPtonCA130_provenance.
- NP1246897.RAnkx872aJV5uZUXjRy_q0J8qFzCunug_GqRpBgPtonCA130_assertion description "[Genetic associations of Nrf2-encoding NFE2L2 variants with Parkinson's disease - a multicenter study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1246897.RAnkx872aJV5uZUXjRy_q0J8qFzCunug_GqRpBgPtonCA130_provenance.
- NP1246897.RAnkx872aJV5uZUXjRy_q0J8qFzCunug_GqRpBgPtonCA130_assertion evidence source_evidence_literature NP1246897.RAnkx872aJV5uZUXjRy_q0J8qFzCunug_GqRpBgPtonCA130_provenance.
- NP1246897.RAnkx872aJV5uZUXjRy_q0J8qFzCunug_GqRpBgPtonCA130_assertion SIO_000772 25496089 NP1246897.RAnkx872aJV5uZUXjRy_q0J8qFzCunug_GqRpBgPtonCA130_provenance.
- NP1246897.RAnkx872aJV5uZUXjRy_q0J8qFzCunug_GqRpBgPtonCA130_assertion wasDerivedFrom befree-2016 NP1246897.RAnkx872aJV5uZUXjRy_q0J8qFzCunug_GqRpBgPtonCA130_provenance.
- NP1246897.RAnkx872aJV5uZUXjRy_q0J8qFzCunug_GqRpBgPtonCA130_assertion wasGeneratedBy ECO_0000203 NP1246897.RAnkx872aJV5uZUXjRy_q0J8qFzCunug_GqRpBgPtonCA130_provenance.
- befree-2016 importedOn "2016-02-19" NP1246897.RAnkx872aJV5uZUXjRy_q0J8qFzCunug_GqRpBgPtonCA130_provenance.