Matches in Nanopublications for { ?s ?p "[The TYR haplotype carrying only the Arg402Gln variant allele was significantly associated with SCC risk (OR, 1.35; 95% CI, 1.04-1.74).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[The TYR haplotype carrying only the Arg402Gln variant allele was significantly associated with SCC risk (OR, 1.35; 95% CI, 1.04-1.74).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[The TYR haplotype carrying only the Arg402Gln variant allele was significantly associated with SCC risk (OR, 1.35; 95% CI, 1.04-1.74).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP763888.RAgTFGSG0hOKF4oLfPglRfuS5kEiXwQ0mHeYQvRRYjM7o130_assertion description "[The TYR haplotype carrying only the Arg402Gln variant allele was significantly associated with SCC risk (OR, 1.35; 95% CI, 1.04-1.74).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP763888.RAgTFGSG0hOKF4oLfPglRfuS5kEiXwQ0mHeYQvRRYjM7o130_provenance.
- NP120508.RAPoe2jOFKm_GhqcI5pAFBbg3OuPa0DFZvmtdRkdgogYA130_assertion description "[The TYR haplotype carrying only the Arg402Gln variant allele was significantly associated with SCC risk (OR, 1.35; 95% CI, 1.04-1.74).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120508.RAPoe2jOFKm_GhqcI5pAFBbg3OuPa0DFZvmtdRkdgogYA130_provenance.
- NP734011.RAMNF1cH_2yOaIZjJG_pUQlbDK7hkJTiuywHBPs-xKgdo130_assertion description "[The TYR haplotype carrying only the Arg402Gln variant allele was significantly associated with SCC risk (OR, 1.35; 95% CI, 1.04-1.74).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP734011.RAMNF1cH_2yOaIZjJG_pUQlbDK7hkJTiuywHBPs-xKgdo130_provenance.
- NP145934.RAzlkaSfxt7r4VaOEMzVG0qfEWaBa04lzBye1w-Zchh28130_assertion description "[The TYR haplotype carrying only the Arg402Gln variant allele was significantly associated with SCC risk (OR, 1.35; 95% CI, 1.04-1.74).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145934.RAzlkaSfxt7r4VaOEMzVG0qfEWaBa04lzBye1w-Zchh28130_provenance.