Matches in Nanopublications for { ?s ?p "[The ALDH2 Lys and XRCC1 Gln variant alleles were associated with an increased risk of ESCC with adjusted ORs of 1.91 (95% CI, 0.96-3.80) and 1.67 (95% CI, 1.08-2.59), respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP33914.RAgQmiytXnfyWBVZ-hZjAgJQfgz31hJvirE6wFI24maVU130_assertion description "[The ALDH2 Lys and XRCC1 Gln variant alleles were associated with an increased risk of ESCC with adjusted ORs of 1.91 (95% CI, 0.96-3.80) and 1.67 (95% CI, 1.08-2.59), respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP33914.RAgQmiytXnfyWBVZ-hZjAgJQfgz31hJvirE6wFI24maVU130_provenance.
- NP8409.RAsw3PxcRmlRyIk4KWrTpCU2eiIlUdKxyc45c9ryGPUfg130_assertion description "[The ALDH2 Lys and XRCC1 Gln variant alleles were associated with an increased risk of ESCC with adjusted ORs of 1.91 (95% CI, 0.96-3.80) and 1.67 (95% CI, 1.08-2.59), respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP8409.RAsw3PxcRmlRyIk4KWrTpCU2eiIlUdKxyc45c9ryGPUfg130_provenance.