Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP177759.RANoDKziu8vjNzlwDFtunfXCTHDdtqxCkDnMmv2dqxJek130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP177759.RANoDKziu8vjNzlwDFtunfXCTHDdtqxCkDnMmv2dqxJek130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP177759.RANoDKziu8vjNzlwDFtunfXCTHDdtqxCkDnMmv2dqxJek130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP177759.RANoDKziu8vjNzlwDFtunfXCTHDdtqxCkDnMmv2dqxJek130_provenance.
- NP177759.RANoDKziu8vjNzlwDFtunfXCTHDdtqxCkDnMmv2dqxJek130_assertion description "[We examined frequencies of the M235T variant of angiotensinogen gene and I/D polymorphism of gene for angiotensin-converting enzyme in Slovak population: in hypertensive patients, coronary heart disease (CHD), dilated cardiomyopathy (DCM) and myocardial infarction (MI) patients compared to healthy subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177759.RANoDKziu8vjNzlwDFtunfXCTHDdtqxCkDnMmv2dqxJek130_provenance.
- NP177759.RANoDKziu8vjNzlwDFtunfXCTHDdtqxCkDnMmv2dqxJek130_assertion evidence source_evidence_literature NP177759.RANoDKziu8vjNzlwDFtunfXCTHDdtqxCkDnMmv2dqxJek130_provenance.
- NP177759.RANoDKziu8vjNzlwDFtunfXCTHDdtqxCkDnMmv2dqxJek130_assertion SIO_000772 17579251 NP177759.RANoDKziu8vjNzlwDFtunfXCTHDdtqxCkDnMmv2dqxJek130_provenance.
- NP177759.RANoDKziu8vjNzlwDFtunfXCTHDdtqxCkDnMmv2dqxJek130_assertion wasDerivedFrom befree-20140225 NP177759.RANoDKziu8vjNzlwDFtunfXCTHDdtqxCkDnMmv2dqxJek130_provenance.
- NP177759.RANoDKziu8vjNzlwDFtunfXCTHDdtqxCkDnMmv2dqxJek130_assertion wasGeneratedBy ECO_0000203 NP177759.RANoDKziu8vjNzlwDFtunfXCTHDdtqxCkDnMmv2dqxJek130_provenance.
- befree-20140225 importedOn "2014-02-25" NP177759.RANoDKziu8vjNzlwDFtunfXCTHDdtqxCkDnMmv2dqxJek130_provenance.