Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP72670.RAk3UEAynE5TZ75eI3HlSNpRqz26tQDD7a_wng60e-AwI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP72670.RAk3UEAynE5TZ75eI3HlSNpRqz26tQDD7a_wng60e-AwI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP72670.RAk3UEAynE5TZ75eI3HlSNpRqz26tQDD7a_wng60e-AwI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP72670.RAk3UEAynE5TZ75eI3HlSNpRqz26tQDD7a_wng60e-AwI130_provenance.
- NP72670.RAk3UEAynE5TZ75eI3HlSNpRqz26tQDD7a_wng60e-AwI130_assertion description "[These results provide evidence of a significant role for genetic variation at the IFNG locus and provide detailed understanding of the genetic mechanisms underlying this association.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP72670.RAk3UEAynE5TZ75eI3HlSNpRqz26tQDD7a_wng60e-AwI130_provenance.
- NP72670.RAk3UEAynE5TZ75eI3HlSNpRqz26tQDD7a_wng60e-AwI130_assertion evidence source_evidence_literature NP72670.RAk3UEAynE5TZ75eI3HlSNpRqz26tQDD7a_wng60e-AwI130_provenance.
- NP72670.RAk3UEAynE5TZ75eI3HlSNpRqz26tQDD7a_wng60e-AwI130_assertion SIO_000772 16690980 NP72670.RAk3UEAynE5TZ75eI3HlSNpRqz26tQDD7a_wng60e-AwI130_provenance.
- NP72670.RAk3UEAynE5TZ75eI3HlSNpRqz26tQDD7a_wng60e-AwI130_assertion wasDerivedFrom gad-20150221 NP72670.RAk3UEAynE5TZ75eI3HlSNpRqz26tQDD7a_wng60e-AwI130_provenance.
- NP72670.RAk3UEAynE5TZ75eI3HlSNpRqz26tQDD7a_wng60e-AwI130_assertion wasGeneratedBy ECO_0000203 NP72670.RAk3UEAynE5TZ75eI3HlSNpRqz26tQDD7a_wng60e-AwI130_provenance.
- gad-20150221 importedOn "2015-02-21" NP72670.RAk3UEAynE5TZ75eI3HlSNpRqz26tQDD7a_wng60e-AwI130_provenance.