Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP620028.RAX9fIV3SDI4POVw24rU-V644xQAGVRYTDhTkl4fgjJbY130_assertion> ?p ?o ?g. }
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- NP620028.RAX9fIV3SDI4POVw24rU-V644xQAGVRYTDhTkl4fgjJbY130_assertion type Assertion NP620028.RAX9fIV3SDI4POVw24rU-V644xQAGVRYTDhTkl4fgjJbY130_head.
- NP620028.RAX9fIV3SDI4POVw24rU-V644xQAGVRYTDhTkl4fgjJbY130_assertion description "[Alpha-1-antitrypsin (A1AT) deficiency is an autosomal hereditary disorder associated with a major reduction in serum A1AT levels.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP620028.RAX9fIV3SDI4POVw24rU-V644xQAGVRYTDhTkl4fgjJbY130_provenance.
- NP620028.RAX9fIV3SDI4POVw24rU-V644xQAGVRYTDhTkl4fgjJbY130_assertion evidence source_evidence_literature NP620028.RAX9fIV3SDI4POVw24rU-V644xQAGVRYTDhTkl4fgjJbY130_provenance.
- NP620028.RAX9fIV3SDI4POVw24rU-V644xQAGVRYTDhTkl4fgjJbY130_assertion SIO_000772 3289385 NP620028.RAX9fIV3SDI4POVw24rU-V644xQAGVRYTDhTkl4fgjJbY130_provenance.
- NP620028.RAX9fIV3SDI4POVw24rU-V644xQAGVRYTDhTkl4fgjJbY130_assertion wasDerivedFrom befree-20150227 NP620028.RAX9fIV3SDI4POVw24rU-V644xQAGVRYTDhTkl4fgjJbY130_provenance.
- NP620028.RAX9fIV3SDI4POVw24rU-V644xQAGVRYTDhTkl4fgjJbY130_assertion wasGeneratedBy ECO_0000203 NP620028.RAX9fIV3SDI4POVw24rU-V644xQAGVRYTDhTkl4fgjJbY130_provenance.