Matches in Nanopublications for { ?s ?p "[α-1 antitrypsin (AAT) deficiency is one of the most important genetic causes of childhood liver diseases in some parts of the world, but its geographic distribution is highly variable.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP619849.RACd1UdKOcMcdaUSH9r-U0Dzz-Z1O8eL4jWCHVIkf0_Wc130_assertion description "[α-1 antitrypsin (AAT) deficiency is one of the most important genetic causes of childhood liver diseases in some parts of the world, but its geographic distribution is highly variable.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP619849.RACd1UdKOcMcdaUSH9r-U0Dzz-Z1O8eL4jWCHVIkf0_Wc130_provenance.
- NP1039138.RA4WOQFSdy5S6SkWStkqxA2kjhxBAvV3WFnng-IEd0gro130_assertion description "[α-1 antitrypsin (AAT) deficiency is one of the most important genetic causes of childhood liver diseases in some parts of the world, but its geographic distribution is highly variable.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1039138.RA4WOQFSdy5S6SkWStkqxA2kjhxBAvV3WFnng-IEd0gro130_provenance.
- NP1039139.RAKbBlxBcRQXEYG_daHvIW7dhtKRhaVlozrUlt9LRBIbc130_assertion description "[α-1 antitrypsin (AAT) deficiency is one of the most important genetic causes of childhood liver diseases in some parts of the world, but its geographic distribution is highly variable.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1039139.RAKbBlxBcRQXEYG_daHvIW7dhtKRhaVlozrUlt9LRBIbc130_provenance.