Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP914058.RAEJLX9J-4fTwZUHTZd-OuMfg783yQfIGF3VGEGVwtkhI130_assertion> ?p ?o ?g. }
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- NP914058.RAEJLX9J-4fTwZUHTZd-OuMfg783yQfIGF3VGEGVwtkhI130_assertion type Assertion NP914058.RAEJLX9J-4fTwZUHTZd-OuMfg783yQfIGF3VGEGVwtkhI130_head.
- NP914058.RAEJLX9J-4fTwZUHTZd-OuMfg783yQfIGF3VGEGVwtkhI130_assertion description "[Previously, we discovered 3 polymorphisms in the prostacyclin synthase (PGIS) gene: 1) T-192G, in the 5-flanking region, a novel single-nucleotide polymorphism (SNP) that is not associated with essential hypertension (EH); 2) a variable number of tandem repeat (VNTR) polymorphism, 6 nucleotides upstream from the ATG start codon, that is associated with risk of cerebral infarction; and 3) C1117A, in exon 8, an SNP that does not cause an amino acid change in codon 373, and that is associated with risk of myocardial infarction (MI).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP914058.RAEJLX9J-4fTwZUHTZd-OuMfg783yQfIGF3VGEGVwtkhI130_provenance.
- NP914058.RAEJLX9J-4fTwZUHTZd-OuMfg783yQfIGF3VGEGVwtkhI130_assertion evidence source_evidence_literature NP914058.RAEJLX9J-4fTwZUHTZd-OuMfg783yQfIGF3VGEGVwtkhI130_provenance.
- NP914058.RAEJLX9J-4fTwZUHTZd-OuMfg783yQfIGF3VGEGVwtkhI130_assertion SIO_000772 12924623 NP914058.RAEJLX9J-4fTwZUHTZd-OuMfg783yQfIGF3VGEGVwtkhI130_provenance.
- NP914058.RAEJLX9J-4fTwZUHTZd-OuMfg783yQfIGF3VGEGVwtkhI130_assertion wasDerivedFrom befree-20140225 NP914058.RAEJLX9J-4fTwZUHTZd-OuMfg783yQfIGF3VGEGVwtkhI130_provenance.
- NP914058.RAEJLX9J-4fTwZUHTZd-OuMfg783yQfIGF3VGEGVwtkhI130_assertion wasGeneratedBy ECO_0000203 NP914058.RAEJLX9J-4fTwZUHTZd-OuMfg783yQfIGF3VGEGVwtkhI130_provenance.