Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP51660.RA0WCJNCC-TyiUbrpj3x7qfGK1rdoxDVE9nc4ROafC4eY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP51660.RA0WCJNCC-TyiUbrpj3x7qfGK1rdoxDVE9nc4ROafC4eY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP51660.RA0WCJNCC-TyiUbrpj3x7qfGK1rdoxDVE9nc4ROafC4eY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP51660.RA0WCJNCC-TyiUbrpj3x7qfGK1rdoxDVE9nc4ROafC4eY130_provenance.
- NP51660.RA0WCJNCC-TyiUbrpj3x7qfGK1rdoxDVE9nc4ROafC4eY130_assertion description "[Collectively, our results suggest that the 1672T variant of the OCTN1 gene and the -207C variant of the OCTN2 gene represent risk factors for CD in the Greek population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51660.RA0WCJNCC-TyiUbrpj3x7qfGK1rdoxDVE9nc4ROafC4eY130_provenance.
- NP51660.RA0WCJNCC-TyiUbrpj3x7qfGK1rdoxDVE9nc4ROafC4eY130_assertion evidence source_evidence_literature NP51660.RA0WCJNCC-TyiUbrpj3x7qfGK1rdoxDVE9nc4ROafC4eY130_provenance.
- NP51660.RA0WCJNCC-TyiUbrpj3x7qfGK1rdoxDVE9nc4ROafC4eY130_assertion SIO_000772 16437728 NP51660.RA0WCJNCC-TyiUbrpj3x7qfGK1rdoxDVE9nc4ROafC4eY130_provenance.
- NP51660.RA0WCJNCC-TyiUbrpj3x7qfGK1rdoxDVE9nc4ROafC4eY130_assertion wasDerivedFrom gad-20130706 NP51660.RA0WCJNCC-TyiUbrpj3x7qfGK1rdoxDVE9nc4ROafC4eY130_provenance.
- NP51660.RA0WCJNCC-TyiUbrpj3x7qfGK1rdoxDVE9nc4ROafC4eY130_assertion wasGeneratedBy ECO_0000203 NP51660.RA0WCJNCC-TyiUbrpj3x7qfGK1rdoxDVE9nc4ROafC4eY130_provenance.
- gad-20130706 importedOn "2013-07-06" NP51660.RA0WCJNCC-TyiUbrpj3x7qfGK1rdoxDVE9nc4ROafC4eY130_provenance.