Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP619204.RAnsQT2NkFj_a7DPoe7zXs9a7ja7SuVM-lEWHJBRei97g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP619204.RAnsQT2NkFj_a7DPoe7zXs9a7ja7SuVM-lEWHJBRei97g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP619204.RAnsQT2NkFj_a7DPoe7zXs9a7ja7SuVM-lEWHJBRei97g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP619204.RAnsQT2NkFj_a7DPoe7zXs9a7ja7SuVM-lEWHJBRei97g130_provenance.
- NP619204.RAnsQT2NkFj_a7DPoe7zXs9a7ja7SuVM-lEWHJBRei97g130_assertion description "[Single-SNP analysis demonstrated significant associations of the CARD15_R702W variation and the NALP12_In9 T-allele with AD (P = 0.008 and P = 0.03, resp.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP619204.RAnsQT2NkFj_a7DPoe7zXs9a7ja7SuVM-lEWHJBRei97g130_provenance.
- NP619204.RAnsQT2NkFj_a7DPoe7zXs9a7ja7SuVM-lEWHJBRei97g130_assertion evidence source_evidence_literature NP619204.RAnsQT2NkFj_a7DPoe7zXs9a7ja7SuVM-lEWHJBRei97g130_provenance.
- NP619204.RAnsQT2NkFj_a7DPoe7zXs9a7ja7SuVM-lEWHJBRei97g130_assertion SIO_000772 17620097 NP619204.RAnsQT2NkFj_a7DPoe7zXs9a7ja7SuVM-lEWHJBRei97g130_provenance.
- NP619204.RAnsQT2NkFj_a7DPoe7zXs9a7ja7SuVM-lEWHJBRei97g130_assertion wasDerivedFrom befree-2016 NP619204.RAnsQT2NkFj_a7DPoe7zXs9a7ja7SuVM-lEWHJBRei97g130_provenance.
- NP619204.RAnsQT2NkFj_a7DPoe7zXs9a7ja7SuVM-lEWHJBRei97g130_assertion wasGeneratedBy ECO_0000203 NP619204.RAnsQT2NkFj_a7DPoe7zXs9a7ja7SuVM-lEWHJBRei97g130_provenance.
- befree-2016 importedOn "2016-02-19" NP619204.RAnsQT2NkFj_a7DPoe7zXs9a7ja7SuVM-lEWHJBRei97g130_provenance.