Matches in Nanopublications for { ?s ?p "[Our data suggest that CYP19 VNTR (TTTA)(10) allele as well as the combined genotype CYP1A1 m1 polymorphism and GSTM1 null deletion associate with the endometriosis phenotype, whereas the GSTT1 null deletion does not.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP62783.RAAc5GI9Lrl-ChGRXaywKe_7Anb8pyv7pOCyawAXEkW_w130_assertion description "[Our data suggest that CYP19 VNTR (TTTA)(10) allele as well as the combined genotype CYP1A1 m1 polymorphism and GSTM1 null deletion associate with the endometriosis phenotype, whereas the GSTT1 null deletion does not.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP62783.RAAc5GI9Lrl-ChGRXaywKe_7Anb8pyv7pOCyawAXEkW_w130_provenance.
- NP339311.RAx65U9z_bJFThlt7hQQXDoIF5K80SRdGMqdEy-vlKC3U130_assertion description "[Our data suggest that CYP19 VNTR (TTTA)(10) allele as well as the combined genotype CYP1A1 m1 polymorphism and GSTM1 null deletion associate with the endometriosis phenotype, whereas the GSTT1 null deletion does not.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP339311.RAx65U9z_bJFThlt7hQQXDoIF5K80SRdGMqdEy-vlKC3U130_provenance.
- assertion description "[Our data suggest that CYP19 VNTR (TTTA)(10) allele as well as the combined genotype CYP1A1 m1 polymorphism and GSTM1 null deletion associate with the endometriosis phenotype, whereas the GSTT1 null deletion does not.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Our data suggest that CYP19 VNTR (TTTA)(10) allele as well as the combined genotype CYP1A1 m1 polymorphism and GSTM1 null deletion associate with the endometriosis phenotype, whereas the GSTT1 null deletion does not.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Our data suggest that CYP19 VNTR (TTTA)(10) allele as well as the combined genotype CYP1A1 m1 polymorphism and GSTM1 null deletion associate with the endometriosis phenotype, whereas the GSTT1 null deletion does not.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP78624.RA25ddy_W-Zg6RrjDPYxtGYJ6P7CFbIoAg-TACrW2CT3k130_assertion description "[Our data suggest that CYP19 VNTR (TTTA)(10) allele as well as the combined genotype CYP1A1 m1 polymorphism and GSTM1 null deletion associate with the endometriosis phenotype, whereas the GSTT1 null deletion does not.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78624.RA25ddy_W-Zg6RrjDPYxtGYJ6P7CFbIoAg-TACrW2CT3k130_provenance.
- NP81408.RAp4rSUCLGxuHOElgW0-k1I5V0ScTL4_ULTRjUqdWVJiw130_assertion description "[Our data suggest that CYP19 VNTR (TTTA)(10) allele as well as the combined genotype CYP1A1 m1 polymorphism and GSTM1 null deletion associate with the endometriosis phenotype, whereas the GSTT1 null deletion does not.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81408.RAp4rSUCLGxuHOElgW0-k1I5V0ScTL4_ULTRjUqdWVJiw130_provenance.
- NP385964.RAYHgEnkUmOaNGJIZQt_AGGPpZzSAKjDZTUPTGOiSHmkc130_assertion description "[Our data suggest that CYP19 VNTR (TTTA)(10) allele as well as the combined genotype CYP1A1 m1 polymorphism and GSTM1 null deletion associate with the endometriosis phenotype, whereas the GSTT1 null deletion does not.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP385964.RAYHgEnkUmOaNGJIZQt_AGGPpZzSAKjDZTUPTGOiSHmkc130_provenance.
- NP385965.RAYiEEYYdY830MNnVhbFVNKCl-QeP5VHT3MP6ajaxC0rg130_assertion description "[Our data suggest that CYP19 VNTR (TTTA)(10) allele as well as the combined genotype CYP1A1 m1 polymorphism and GSTM1 null deletion associate with the endometriosis phenotype, whereas the GSTT1 null deletion does not.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP385965.RAYiEEYYdY830MNnVhbFVNKCl-QeP5VHT3MP6ajaxC0rg130_provenance.
- NP385966.RAdv3yyIWWgdDlruVfMNSSrhmt8TZcFgl6fsrz5AnKxaI130_assertion description "[Our data suggest that CYP19 VNTR (TTTA)(10) allele as well as the combined genotype CYP1A1 m1 polymorphism and GSTM1 null deletion associate with the endometriosis phenotype, whereas the GSTT1 null deletion does not.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP385966.RAdv3yyIWWgdDlruVfMNSSrhmt8TZcFgl6fsrz5AnKxaI130_provenance.