Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP211939.RAd0LrtCQgwQ9o33uiZ2CuWSwbmxgpJwery07xjl1yYoA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP211939.RAd0LrtCQgwQ9o33uiZ2CuWSwbmxgpJwery07xjl1yYoA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP211939.RAd0LrtCQgwQ9o33uiZ2CuWSwbmxgpJwery07xjl1yYoA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP211939.RAd0LrtCQgwQ9o33uiZ2CuWSwbmxgpJwery07xjl1yYoA130_provenance.
- NP211939.RAd0LrtCQgwQ9o33uiZ2CuWSwbmxgpJwery07xjl1yYoA130_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." NP211939.RAd0LrtCQgwQ9o33uiZ2CuWSwbmxgpJwery07xjl1yYoA130_provenance.
- NP211939.RAd0LrtCQgwQ9o33uiZ2CuWSwbmxgpJwery07xjl1yYoA130_assertion evidence source_evidence_literature NP211939.RAd0LrtCQgwQ9o33uiZ2CuWSwbmxgpJwery07xjl1yYoA130_provenance.
- NP211939.RAd0LrtCQgwQ9o33uiZ2CuWSwbmxgpJwery07xjl1yYoA130_assertion SIO_000772 15098605 NP211939.RAd0LrtCQgwQ9o33uiZ2CuWSwbmxgpJwery07xjl1yYoA130_provenance.
- NP211939.RAd0LrtCQgwQ9o33uiZ2CuWSwbmxgpJwery07xjl1yYoA130_assertion wasDerivedFrom befree-20140225 NP211939.RAd0LrtCQgwQ9o33uiZ2CuWSwbmxgpJwery07xjl1yYoA130_provenance.
- NP211939.RAd0LrtCQgwQ9o33uiZ2CuWSwbmxgpJwery07xjl1yYoA130_assertion wasGeneratedBy ECO_0000203 NP211939.RAd0LrtCQgwQ9o33uiZ2CuWSwbmxgpJwery07xjl1yYoA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP211939.RAd0LrtCQgwQ9o33uiZ2CuWSwbmxgpJwery07xjl1yYoA130_provenance.