Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP101788.RA4xhzxi3_ZN224drQYbV3UiZCmm1Luzjxnev1Z0oheqc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP101788.RA4xhzxi3_ZN224drQYbV3UiZCmm1Luzjxnev1Z0oheqc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP101788.RA4xhzxi3_ZN224drQYbV3UiZCmm1Luzjxnev1Z0oheqc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP101788.RA4xhzxi3_ZN224drQYbV3UiZCmm1Luzjxnev1Z0oheqc130_provenance.
- NP101788.RA4xhzxi3_ZN224drQYbV3UiZCmm1Luzjxnev1Z0oheqc130_assertion description "[The frequency of subject with the homozygote of 12 repeat allele was significantly higher in patients with hypertension compared with control subjects (987 cases, 924 controls) (P=0.030; odds ratio=1.24) at a novel VNTR polymorphism of CIAS1 intron 4 loci.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP101788.RA4xhzxi3_ZN224drQYbV3UiZCmm1Luzjxnev1Z0oheqc130_provenance.
- NP101788.RA4xhzxi3_ZN224drQYbV3UiZCmm1Luzjxnev1Z0oheqc130_assertion evidence source_evidence_literature NP101788.RA4xhzxi3_ZN224drQYbV3UiZCmm1Luzjxnev1Z0oheqc130_provenance.
- NP101788.RA4xhzxi3_ZN224drQYbV3UiZCmm1Luzjxnev1Z0oheqc130_assertion SIO_000772 16868559 NP101788.RA4xhzxi3_ZN224drQYbV3UiZCmm1Luzjxnev1Z0oheqc130_provenance.
- NP101788.RA4xhzxi3_ZN224drQYbV3UiZCmm1Luzjxnev1Z0oheqc130_assertion wasDerivedFrom gad-20150221 NP101788.RA4xhzxi3_ZN224drQYbV3UiZCmm1Luzjxnev1Z0oheqc130_provenance.
- NP101788.RA4xhzxi3_ZN224drQYbV3UiZCmm1Luzjxnev1Z0oheqc130_assertion wasGeneratedBy ECO_0000203 NP101788.RA4xhzxi3_ZN224drQYbV3UiZCmm1Luzjxnev1Z0oheqc130_provenance.
- gad-20150221 importedOn "2015-02-21" NP101788.RA4xhzxi3_ZN224drQYbV3UiZCmm1Luzjxnev1Z0oheqc130_provenance.