Matches in Nanopublications for { ?s ?p "[Alpha-1 antitrypsin (AAT) deficiency is a hereditary disorder characterized by an early onset of emphysema.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP211939.RAd0LrtCQgwQ9o33uiZ2CuWSwbmxgpJwery07xjl1yYoA130_assertion description "[Alpha-1 antitrypsin (AAT) deficiency is a hereditary disorder characterized by an early onset of emphysema.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP211939.RAd0LrtCQgwQ9o33uiZ2CuWSwbmxgpJwery07xjl1yYoA130_provenance.
- assertion description "[Alpha-1 antitrypsin (AAT) deficiency is a hereditary disorder characterized by an early onset of emphysema.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP440823.RAOBIjq4yl9VY7LjOle2wCLNpaZwzVf26Wv7Q-X74bhmw130_assertion description "[Alpha-1 antitrypsin (AAT) deficiency is a hereditary disorder characterized by an early onset of emphysema.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP440823.RAOBIjq4yl9VY7LjOle2wCLNpaZwzVf26Wv7Q-X74bhmw130_provenance.