Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP440823.RAOBIjq4yl9VY7LjOle2wCLNpaZwzVf26Wv7Q-X74bhmw130_assertion> ?p ?o ?g. }
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- NP440823.RAOBIjq4yl9VY7LjOle2wCLNpaZwzVf26Wv7Q-X74bhmw130_assertion type Assertion NP440823.RAOBIjq4yl9VY7LjOle2wCLNpaZwzVf26Wv7Q-X74bhmw130_head.
- 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.
- NP440823.RAOBIjq4yl9VY7LjOle2wCLNpaZwzVf26Wv7Q-X74bhmw130_assertion evidence source_evidence_literature NP440823.RAOBIjq4yl9VY7LjOle2wCLNpaZwzVf26Wv7Q-X74bhmw130_provenance.
- NP440823.RAOBIjq4yl9VY7LjOle2wCLNpaZwzVf26Wv7Q-X74bhmw130_assertion SIO_000772 15098605 NP440823.RAOBIjq4yl9VY7LjOle2wCLNpaZwzVf26Wv7Q-X74bhmw130_provenance.
- NP440823.RAOBIjq4yl9VY7LjOle2wCLNpaZwzVf26Wv7Q-X74bhmw130_assertion wasDerivedFrom befree-2016 NP440823.RAOBIjq4yl9VY7LjOle2wCLNpaZwzVf26Wv7Q-X74bhmw130_provenance.
- NP440823.RAOBIjq4yl9VY7LjOle2wCLNpaZwzVf26Wv7Q-X74bhmw130_assertion wasGeneratedBy ECO_0000203 NP440823.RAOBIjq4yl9VY7LjOle2wCLNpaZwzVf26Wv7Q-X74bhmw130_provenance.