Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP943200.RAQq6XHJP6J-cWIpFkgVZwdtqXIAG5Ng0ZhxggS1hT55s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP943200.RAQq6XHJP6J-cWIpFkgVZwdtqXIAG5Ng0ZhxggS1hT55s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP943200.RAQq6XHJP6J-cWIpFkgVZwdtqXIAG5Ng0ZhxggS1hT55s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP943200.RAQq6XHJP6J-cWIpFkgVZwdtqXIAG5Ng0ZhxggS1hT55s130_provenance.
- NP943200.RAQq6XHJP6J-cWIpFkgVZwdtqXIAG5Ng0ZhxggS1hT55s130_assertion description "[Conversely, homozygous subjects for the variant allele (A) in the GCK gene had significantly lower TAG (GG+GA: 1.48 (SD 0.03) mmol/l v. AA: 1.17 (SD 0.18) mmol/l; P= 0.033) and a higher risk of diabetes (OR 3.3, 95 % CI 1.2, 9.2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP943200.RAQq6XHJP6J-cWIpFkgVZwdtqXIAG5Ng0ZhxggS1hT55s130_provenance.
- NP943200.RAQq6XHJP6J-cWIpFkgVZwdtqXIAG5Ng0ZhxggS1hT55s130_assertion evidence source_evidence_literature NP943200.RAQq6XHJP6J-cWIpFkgVZwdtqXIAG5Ng0ZhxggS1hT55s130_provenance.
- NP943200.RAQq6XHJP6J-cWIpFkgVZwdtqXIAG5Ng0ZhxggS1hT55s130_assertion SIO_000772 22716779 NP943200.RAQq6XHJP6J-cWIpFkgVZwdtqXIAG5Ng0ZhxggS1hT55s130_provenance.
- NP943200.RAQq6XHJP6J-cWIpFkgVZwdtqXIAG5Ng0ZhxggS1hT55s130_assertion wasDerivedFrom befree-20150227 NP943200.RAQq6XHJP6J-cWIpFkgVZwdtqXIAG5Ng0ZhxggS1hT55s130_provenance.
- NP943200.RAQq6XHJP6J-cWIpFkgVZwdtqXIAG5Ng0ZhxggS1hT55s130_assertion wasGeneratedBy ECO_0000203 NP943200.RAQq6XHJP6J-cWIpFkgVZwdtqXIAG5Ng0ZhxggS1hT55s130_provenance.
- befree-20150227 importedOn "2015-02-27" NP943200.RAQq6XHJP6J-cWIpFkgVZwdtqXIAG5Ng0ZhxggS1hT55s130_provenance.