Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP648540.RArz1dlaJdauZFBKHjoqNXoyJEHJeSjkTLqW6DLQGuhHU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP648540.RArz1dlaJdauZFBKHjoqNXoyJEHJeSjkTLqW6DLQGuhHU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP648540.RArz1dlaJdauZFBKHjoqNXoyJEHJeSjkTLqW6DLQGuhHU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP648540.RArz1dlaJdauZFBKHjoqNXoyJEHJeSjkTLqW6DLQGuhHU130_provenance.
- NP648540.RArz1dlaJdauZFBKHjoqNXoyJEHJeSjkTLqW6DLQGuhHU130_assertion description "[In further analyses of incident CHD, genotypes carrying the 402H allele were a significant predictor of incident CHD in whites who had hypertension (402YH: HRR 1.19, 95% CI 1.01-1.40; 402HH: HRR 1.28, 95% CI 1.04-1.57).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP648540.RArz1dlaJdauZFBKHjoqNXoyJEHJeSjkTLqW6DLQGuhHU130_provenance.
- NP648540.RArz1dlaJdauZFBKHjoqNXoyJEHJeSjkTLqW6DLQGuhHU130_assertion evidence source_evidence_literature NP648540.RArz1dlaJdauZFBKHjoqNXoyJEHJeSjkTLqW6DLQGuhHU130_provenance.
- NP648540.RArz1dlaJdauZFBKHjoqNXoyJEHJeSjkTLqW6DLQGuhHU130_assertion SIO_000772 18292760 NP648540.RArz1dlaJdauZFBKHjoqNXoyJEHJeSjkTLqW6DLQGuhHU130_provenance.
- NP648540.RArz1dlaJdauZFBKHjoqNXoyJEHJeSjkTLqW6DLQGuhHU130_assertion wasDerivedFrom befree-20140225 NP648540.RArz1dlaJdauZFBKHjoqNXoyJEHJeSjkTLqW6DLQGuhHU130_provenance.
- NP648540.RArz1dlaJdauZFBKHjoqNXoyJEHJeSjkTLqW6DLQGuhHU130_assertion wasGeneratedBy ECO_0000203 NP648540.RArz1dlaJdauZFBKHjoqNXoyJEHJeSjkTLqW6DLQGuhHU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP648540.RArz1dlaJdauZFBKHjoqNXoyJEHJeSjkTLqW6DLQGuhHU130_provenance.