Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1216713.RA41o0lGGn5GHuV-6VzjLY7VtaD5PdCE2w73lL4Mlcxls130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1216713.RA41o0lGGn5GHuV-6VzjLY7VtaD5PdCE2w73lL4Mlcxls130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1216713.RA41o0lGGn5GHuV-6VzjLY7VtaD5PdCE2w73lL4Mlcxls130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1216713.RA41o0lGGn5GHuV-6VzjLY7VtaD5PdCE2w73lL4Mlcxls130_provenance.
- NP1216713.RA41o0lGGn5GHuV-6VzjLY7VtaD5PdCE2w73lL4Mlcxls130_assertion description "[The HMOX1 genotypes were not found to be associated with CAD, but the short allele carrier group contained more individuals with hsCRP values reflecting low risk of cardiovascular disease in the Korean population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1216713.RA41o0lGGn5GHuV-6VzjLY7VtaD5PdCE2w73lL4Mlcxls130_provenance.
- NP1216713.RA41o0lGGn5GHuV-6VzjLY7VtaD5PdCE2w73lL4Mlcxls130_assertion evidence source_evidence_literature NP1216713.RA41o0lGGn5GHuV-6VzjLY7VtaD5PdCE2w73lL4Mlcxls130_provenance.
- NP1216713.RA41o0lGGn5GHuV-6VzjLY7VtaD5PdCE2w73lL4Mlcxls130_assertion SIO_000772 25187885 NP1216713.RA41o0lGGn5GHuV-6VzjLY7VtaD5PdCE2w73lL4Mlcxls130_provenance.
- NP1216713.RA41o0lGGn5GHuV-6VzjLY7VtaD5PdCE2w73lL4Mlcxls130_assertion wasDerivedFrom befree-2016 NP1216713.RA41o0lGGn5GHuV-6VzjLY7VtaD5PdCE2w73lL4Mlcxls130_provenance.
- NP1216713.RA41o0lGGn5GHuV-6VzjLY7VtaD5PdCE2w73lL4Mlcxls130_assertion wasGeneratedBy ECO_0000203 NP1216713.RA41o0lGGn5GHuV-6VzjLY7VtaD5PdCE2w73lL4Mlcxls130_provenance.
- befree-2016 importedOn "2016-02-19" NP1216713.RA41o0lGGn5GHuV-6VzjLY7VtaD5PdCE2w73lL4Mlcxls130_provenance.