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- source_evidence_literature type ECO_0000212 NP563890.RAH1mA_6RsIlWjvcZvoXl4Jh8WxjAYMgtWyRoh_t_2T9k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP563890.RAH1mA_6RsIlWjvcZvoXl4Jh8WxjAYMgtWyRoh_t_2T9k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP563890.RAH1mA_6RsIlWjvcZvoXl4Jh8WxjAYMgtWyRoh_t_2T9k130_provenance.
- NP563890.RAH1mA_6RsIlWjvcZvoXl4Jh8WxjAYMgtWyRoh_t_2T9k130_assertion description "[Results from the adjusted haplotype-based conditional logistic regression analysis showed a modest association of the PTGER2 2-1-1 haplotype with reduced risk of MI (odds ratio = 0.50, 95% CI; CI = 0.26-0.97, P = 0.04), and the 2-2-1 haplotype with reduced risk of ischemic stroke (odds ratio = 0.68, 95% CI = 0.47-0.99, P = 0.048).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP563890.RAH1mA_6RsIlWjvcZvoXl4Jh8WxjAYMgtWyRoh_t_2T9k130_provenance.
- NP563890.RAH1mA_6RsIlWjvcZvoXl4Jh8WxjAYMgtWyRoh_t_2T9k130_assertion evidence source_evidence_literature NP563890.RAH1mA_6RsIlWjvcZvoXl4Jh8WxjAYMgtWyRoh_t_2T9k130_provenance.
- NP563890.RAH1mA_6RsIlWjvcZvoXl4Jh8WxjAYMgtWyRoh_t_2T9k130_assertion SIO_000772 16879213 NP563890.RAH1mA_6RsIlWjvcZvoXl4Jh8WxjAYMgtWyRoh_t_2T9k130_provenance.
- NP563890.RAH1mA_6RsIlWjvcZvoXl4Jh8WxjAYMgtWyRoh_t_2T9k130_assertion wasDerivedFrom befree-20140225 NP563890.RAH1mA_6RsIlWjvcZvoXl4Jh8WxjAYMgtWyRoh_t_2T9k130_provenance.
- NP563890.RAH1mA_6RsIlWjvcZvoXl4Jh8WxjAYMgtWyRoh_t_2T9k130_assertion wasGeneratedBy ECO_0000203 NP563890.RAH1mA_6RsIlWjvcZvoXl4Jh8WxjAYMgtWyRoh_t_2T9k130_provenance.
- befree-20140225 importedOn "2014-02-25" NP563890.RAH1mA_6RsIlWjvcZvoXl4Jh8WxjAYMgtWyRoh_t_2T9k130_provenance.