Matches in Nanopublications for { ?s ?p "[Alpha-1-antitrypsin (A1AT) deficiency is the most common genetic cause of liver disease in children; however, the role of polymorphic heterogeneity in the A1AT gene as a modifier of other forms of pediatric liver disease is not clear.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Alpha-1-antitrypsin (A1AT) deficiency is the most common genetic cause of liver disease in children; however, the role of polymorphic heterogeneity in the A1AT gene as a modifier of other forms of pediatric liver disease is not clear.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Alpha-1-antitrypsin (A1AT) deficiency is the most common genetic cause of liver disease in children; however, the role of polymorphic heterogeneity in the A1AT gene as a modifier of other forms of pediatric liver disease is not clear.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP587335.RACIGqiabQyFWO4Bu_caglOp1JRQYUCWJB06SRM0D2b6U130_assertion description "[Alpha-1-antitrypsin (A1AT) deficiency is the most common genetic cause of liver disease in children; however, the role of polymorphic heterogeneity in the A1AT gene as a modifier of other forms of pediatric liver disease is not clear.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP587335.RACIGqiabQyFWO4Bu_caglOp1JRQYUCWJB06SRM0D2b6U130_provenance.
- NP64833.RA_VuU03G83QCvGhaaspXhiz6jpHLUnhnOELJEZ2G4uOM130_assertion description "[Alpha-1-antitrypsin (A1AT) deficiency is the most common genetic cause of liver disease in children; however, the role of polymorphic heterogeneity in the A1AT gene as a modifier of other forms of pediatric liver disease is not clear.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP64833.RA_VuU03G83QCvGhaaspXhiz6jpHLUnhnOELJEZ2G4uOM130_provenance.
- NP104785.RAuNHWNIZQvHLc-K-ADqEIxgXHRAbT5joYyGiNqdlTz3A130_assertion description "[Alpha-1-antitrypsin (A1AT) deficiency is the most common genetic cause of liver disease in children; however, the role of polymorphic heterogeneity in the A1AT gene as a modifier of other forms of pediatric liver disease is not clear.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP104785.RAuNHWNIZQvHLc-K-ADqEIxgXHRAbT5joYyGiNqdlTz3A130_provenance.