Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP620028.RAX9fIV3SDI4POVw24rU-V644xQAGVRYTDhTkl4fgjJbY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP620028.RAX9fIV3SDI4POVw24rU-V644xQAGVRYTDhTkl4fgjJbY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP620028.RAX9fIV3SDI4POVw24rU-V644xQAGVRYTDhTkl4fgjJbY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP620028.RAX9fIV3SDI4POVw24rU-V644xQAGVRYTDhTkl4fgjJbY130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP620028.RAX9fIV3SDI4POVw24rU-V644xQAGVRYTDhTkl4fgjJbY130_provenance.