Matches in Nanopublications for { ?s ?p "[Although none of the tested gene polymorphisms was significantly related to an increased risk of COPD alone, our results suggest that the homozygous exon 3 mutant variant of EPHX1 gene in the combination with GSTM1 null genotype is a significant predictor]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP42771.RAH_9uq7q9XsR3unhVSIJsqia6c770_lqOyHc5MnCgj9E130_assertion description "[Although none of the tested gene polymorphisms was significantly related to an increased risk of COPD alone, our results suggest that the homozygous exon 3 mutant variant of EPHX1 gene in the combination with GSTM1 null genotype is a significant predictor]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP42771.RAH_9uq7q9XsR3unhVSIJsqia6c770_lqOyHc5MnCgj9E130_provenance.
- assertion description "[Although none of the tested gene polymorphisms was significantly related to an increased risk of COPD alone, our results suggest that the homozygous exon 3 mutant variant of EPHX1 gene in the combination with GSTM1 null genotype is a significant predictor]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP122771.RAUhQoJ5IeKnX1mAicxGzykG2RgfASbRHZbqoqXZkmwlU130_assertion description "[Although none of the tested gene polymorphisms was significantly related to an increased risk of COPD alone, our results suggest that the homozygous exon 3 mutant variant of EPHX1 gene in the combination with GSTM1 null genotype is a significant predictor]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP122771.RAUhQoJ5IeKnX1mAicxGzykG2RgfASbRHZbqoqXZkmwlU130_provenance.
- NP50442.RAK3kGH2tiqrcD28_ejgQO-RAWpMEA8Ho42Gd1FWIdAYs130_assertion description "[Although none of the tested gene polymorphisms was significantly related to an increased risk of COPD alone, our results suggest that the homozygous exon 3 mutant variant of EPHX1 gene in the combination with GSTM1 null genotype is a significant predictor]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50442.RAK3kGH2tiqrcD28_ejgQO-RAWpMEA8Ho42Gd1FWIdAYs130_provenance.