Matches in Nanopublications for { ?s ?p "[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."@en ?g. }
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- NP477702.RATaKZUPS6WuMLQLm9sxzUOLiZ8ktFvuPesVb8cjOPAxI130_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." NP477702.RATaKZUPS6WuMLQLm9sxzUOLiZ8ktFvuPesVb8cjOPAxI130_provenance.
- NP85264.RAR8GiYvjZ2NSzPk5DZpoavm_W7eDpDO30qm7Tu3w_bwc130_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." NP85264.RAR8GiYvjZ2NSzPk5DZpoavm_W7eDpDO30qm7Tu3w_bwc130_provenance.
- 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." provenance.
- NP561433.RASE2o3Di9kLECh8akjfxujpiN2ElPXIi4Mgduq0c_uDY130_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." NP561433.RASE2o3Di9kLECh8akjfxujpiN2ElPXIi4Mgduq0c_uDY130_provenance.
- NP964588.RALSh6Fp8m0x-hwpeWuepUsl7RV0V8HbRIw1_QPQFDuzY130_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." NP964588.RALSh6Fp8m0x-hwpeWuepUsl7RV0V8HbRIw1_QPQFDuzY130_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.