Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP157761.RAnX8-o5GlvkR1j4D79L1_D0f-mVeVRMc7yiG0tP4BG04130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP157761.RAnX8-o5GlvkR1j4D79L1_D0f-mVeVRMc7yiG0tP4BG04130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP157761.RAnX8-o5GlvkR1j4D79L1_D0f-mVeVRMc7yiG0tP4BG04130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP157761.RAnX8-o5GlvkR1j4D79L1_D0f-mVeVRMc7yiG0tP4BG04130_provenance.
- NP157761.RAnX8-o5GlvkR1j4D79L1_D0f-mVeVRMc7yiG0tP4BG04130_assertion description "[Since the presence of the rs2304052 C allele is associated with an increased risk (odds ratio: 2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP157761.RAnX8-o5GlvkR1j4D79L1_D0f-mVeVRMc7yiG0tP4BG04130_provenance.
- NP157761.RAnX8-o5GlvkR1j4D79L1_D0f-mVeVRMc7yiG0tP4BG04130_assertion evidence source_evidence_literature NP157761.RAnX8-o5GlvkR1j4D79L1_D0f-mVeVRMc7yiG0tP4BG04130_provenance.
- NP157761.RAnX8-o5GlvkR1j4D79L1_D0f-mVeVRMc7yiG0tP4BG04130_assertion SIO_000772 19817957 NP157761.RAnX8-o5GlvkR1j4D79L1_D0f-mVeVRMc7yiG0tP4BG04130_provenance.
- NP157761.RAnX8-o5GlvkR1j4D79L1_D0f-mVeVRMc7yiG0tP4BG04130_assertion wasDerivedFrom gad-20150221 NP157761.RAnX8-o5GlvkR1j4D79L1_D0f-mVeVRMc7yiG0tP4BG04130_provenance.
- NP157761.RAnX8-o5GlvkR1j4D79L1_D0f-mVeVRMc7yiG0tP4BG04130_assertion wasGeneratedBy ECO_0000203 NP157761.RAnX8-o5GlvkR1j4D79L1_D0f-mVeVRMc7yiG0tP4BG04130_provenance.
- gad-20150221 importedOn "2015-02-21" NP157761.RAnX8-o5GlvkR1j4D79L1_D0f-mVeVRMc7yiG0tP4BG04130_provenance.