Matches in Nanopublications for { ?s ?p "[CTLA-4 gene exon-1 +49 A/G polymorphism: lack of association with autoimmune disease in patients with common variable immune deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP481073.RAVJXKUn1zWEqX49iGrEb3B9HSShAMDjpR90cfETu2WWE130_assertion description "[CTLA-4 gene exon-1 +49 A/G polymorphism: lack of association with autoimmune disease in patients with common variable immune deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP481073.RAVJXKUn1zWEqX49iGrEb3B9HSShAMDjpR90cfETu2WWE130_provenance.
- assertion description "[CTLA-4 gene exon-1 +49 A/G polymorphism: lack of association with autoimmune disease in patients with common variable immune deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[CTLA-4 gene exon-1 +49 A/G polymorphism: lack of association with autoimmune disease in patients with common variable immune deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP335182.RATWlqa0-NAg72d_0LqHZYtctaFhW05Ymzp1y_EbFspJE130_assertion description "[CTLA-4 gene exon-1 +49 A/G polymorphism: lack of association with autoimmune disease in patients with common variable immune deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP335182.RATWlqa0-NAg72d_0LqHZYtctaFhW05Ymzp1y_EbFspJE130_provenance.
- NP586318.RAYSWtk5fwfb8DJaOQTgx9tIyencHin3J0OZ_0urqmmiI130_assertion description "[CTLA-4 gene exon-1 +49 A/G polymorphism: lack of association with autoimmune disease in patients with common variable immune deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP586318.RAYSWtk5fwfb8DJaOQTgx9tIyencHin3J0OZ_0urqmmiI130_provenance.
- NP586319.RAgglPvmB80qxSh7V1u-08rhelEbIqFEGrwEhV-WDEqnk130_assertion description "[CTLA-4 gene exon-1 +49 A/G polymorphism: lack of association with autoimmune disease in patients with common variable immune deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP586319.RAgglPvmB80qxSh7V1u-08rhelEbIqFEGrwEhV-WDEqnk130_provenance.