Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP672284.RAsXjWLR2uhZde2UjD5ghOdtU21HNdEDnAV2vjxG45vL4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP672284.RAsXjWLR2uhZde2UjD5ghOdtU21HNdEDnAV2vjxG45vL4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP672284.RAsXjWLR2uhZde2UjD5ghOdtU21HNdEDnAV2vjxG45vL4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP672284.RAsXjWLR2uhZde2UjD5ghOdtU21HNdEDnAV2vjxG45vL4130_provenance.
- NP672284.RAsXjWLR2uhZde2UjD5ghOdtU21HNdEDnAV2vjxG45vL4130_assertion description "[After the adjustment for covariates, the carriers of minor D allele of RGS2-rs34717272 had an increased hypertension risk (DD+ID vs. II; odds ratio=1.19; 95% confidence interval, 1.04-1.35; P value after the Bonferroni correction=0.009 x 5=0.045).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP672284.RAsXjWLR2uhZde2UjD5ghOdtU21HNdEDnAV2vjxG45vL4130_provenance.
- NP672284.RAsXjWLR2uhZde2UjD5ghOdtU21HNdEDnAV2vjxG45vL4130_assertion evidence source_evidence_literature NP672284.RAsXjWLR2uhZde2UjD5ghOdtU21HNdEDnAV2vjxG45vL4130_provenance.
- NP672284.RAsXjWLR2uhZde2UjD5ghOdtU21HNdEDnAV2vjxG45vL4130_assertion SIO_000772 18496125 NP672284.RAsXjWLR2uhZde2UjD5ghOdtU21HNdEDnAV2vjxG45vL4130_provenance.
- NP672284.RAsXjWLR2uhZde2UjD5ghOdtU21HNdEDnAV2vjxG45vL4130_assertion wasDerivedFrom befree-2016 NP672284.RAsXjWLR2uhZde2UjD5ghOdtU21HNdEDnAV2vjxG45vL4130_provenance.
- NP672284.RAsXjWLR2uhZde2UjD5ghOdtU21HNdEDnAV2vjxG45vL4130_assertion wasGeneratedBy ECO_0000203 NP672284.RAsXjWLR2uhZde2UjD5ghOdtU21HNdEDnAV2vjxG45vL4130_provenance.
- befree-2016 importedOn "2016-02-19" NP672284.RAsXjWLR2uhZde2UjD5ghOdtU21HNdEDnAV2vjxG45vL4130_provenance.