Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP619852.RAk38llejfplcI1UWvSI8NxVRMWRwcGtDmwrTj-AIDCGI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP619852.RAk38llejfplcI1UWvSI8NxVRMWRwcGtDmwrTj-AIDCGI130_assertion type Assertion NP619852.RAk38llejfplcI1UWvSI8NxVRMWRwcGtDmwrTj-AIDCGI130_head.
- 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.
- NP619852.RAk38llejfplcI1UWvSI8NxVRMWRwcGtDmwrTj-AIDCGI130_assertion evidence source_evidence_literature NP619852.RAk38llejfplcI1UWvSI8NxVRMWRwcGtDmwrTj-AIDCGI130_provenance.
- NP619852.RAk38llejfplcI1UWvSI8NxVRMWRwcGtDmwrTj-AIDCGI130_assertion SIO_000772 24191907 NP619852.RAk38llejfplcI1UWvSI8NxVRMWRwcGtDmwrTj-AIDCGI130_provenance.
- NP619852.RAk38llejfplcI1UWvSI8NxVRMWRwcGtDmwrTj-AIDCGI130_assertion wasDerivedFrom befree-20150227 NP619852.RAk38llejfplcI1UWvSI8NxVRMWRwcGtDmwrTj-AIDCGI130_provenance.
- NP619852.RAk38llejfplcI1UWvSI8NxVRMWRwcGtDmwrTj-AIDCGI130_assertion wasGeneratedBy ECO_0000203 NP619852.RAk38llejfplcI1UWvSI8NxVRMWRwcGtDmwrTj-AIDCGI130_provenance.