Matches in Nanopublications for { ?s ?p "[Alpha-1 antitrypsin (?1AT) deficiency is a common autosomal recessive disorder characterized by a marked reduction in serum ?1AT levels, lung and liver disease.]. 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 (?1AT) deficiency is a common autosomal recessive disorder characterized by a marked reduction in serum ?1AT levels, lung and liver disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Alpha-1 antitrypsin (?1AT) deficiency is a common autosomal recessive disorder characterized by a marked reduction in serum ?1AT levels, lung and liver disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP619852.RAk38llejfplcI1UWvSI8NxVRMWRwcGtDmwrTj-AIDCGI130_assertion description "[Alpha-1 antitrypsin (?1AT) deficiency is a common autosomal recessive disorder characterized by a marked reduction in serum ?1AT levels, lung and liver disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP619852.RAk38llejfplcI1UWvSI8NxVRMWRwcGtDmwrTj-AIDCGI130_provenance.
- NP1125056.RAi_UWGOCbh3ZdKhDfWcEVeLR-hXVTmpNGby-rHC5F8tE130_assertion description "[Alpha-1 antitrypsin (?1AT) deficiency is a common autosomal recessive disorder characterized by a marked reduction in serum ?1AT levels, lung and liver disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1125056.RAi_UWGOCbh3ZdKhDfWcEVeLR-hXVTmpNGby-rHC5F8tE130_provenance.