Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP435359.RAO9jEE8EfyCocLbYC90OVZGJwGGxrH6wyAzkKspqEG_o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP435359.RAO9jEE8EfyCocLbYC90OVZGJwGGxrH6wyAzkKspqEG_o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP435359.RAO9jEE8EfyCocLbYC90OVZGJwGGxrH6wyAzkKspqEG_o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP435359.RAO9jEE8EfyCocLbYC90OVZGJwGGxrH6wyAzkKspqEG_o130_provenance.
- NP435359.RAO9jEE8EfyCocLbYC90OVZGJwGGxrH6wyAzkKspqEG_o130_assertion description "[Alpha-1-antitrypsin (alpha1antitrypsin) deficiency is a rare hereditary disorder which characteristically presents with emphysema at an early age.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP435359.RAO9jEE8EfyCocLbYC90OVZGJwGGxrH6wyAzkKspqEG_o130_provenance.
- NP435359.RAO9jEE8EfyCocLbYC90OVZGJwGGxrH6wyAzkKspqEG_o130_assertion evidence source_evidence_literature NP435359.RAO9jEE8EfyCocLbYC90OVZGJwGGxrH6wyAzkKspqEG_o130_provenance.
- NP435359.RAO9jEE8EfyCocLbYC90OVZGJwGGxrH6wyAzkKspqEG_o130_assertion SIO_000772 11896901 NP435359.RAO9jEE8EfyCocLbYC90OVZGJwGGxrH6wyAzkKspqEG_o130_provenance.
- NP435359.RAO9jEE8EfyCocLbYC90OVZGJwGGxrH6wyAzkKspqEG_o130_assertion wasDerivedFrom befree-20140225 NP435359.RAO9jEE8EfyCocLbYC90OVZGJwGGxrH6wyAzkKspqEG_o130_provenance.
- NP435359.RAO9jEE8EfyCocLbYC90OVZGJwGGxrH6wyAzkKspqEG_o130_assertion wasGeneratedBy ECO_0000203 NP435359.RAO9jEE8EfyCocLbYC90OVZGJwGGxrH6wyAzkKspqEG_o130_provenance.
- befree-20140225 importedOn "2014-02-25" NP435359.RAO9jEE8EfyCocLbYC90OVZGJwGGxrH6wyAzkKspqEG_o130_provenance.