Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP64833.RA_VuU03G83QCvGhaaspXhiz6jpHLUnhnOELJEZ2G4uOM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP64833.RA_VuU03G83QCvGhaaspXhiz6jpHLUnhnOELJEZ2G4uOM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP64833.RA_VuU03G83QCvGhaaspXhiz6jpHLUnhnOELJEZ2G4uOM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP64833.RA_VuU03G83QCvGhaaspXhiz6jpHLUnhnOELJEZ2G4uOM130_provenance.
- NP64833.RA_VuU03G83QCvGhaaspXhiz6jpHLUnhnOELJEZ2G4uOM130_assertion description "[Alpha-1-antitrypsin (A1AT) deficiency is the most common genetic cause of liver disease in children; however, the role of polymorphic heterogeneity in the A1AT gene as a modifier of other forms of pediatric liver disease is not clear.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP64833.RA_VuU03G83QCvGhaaspXhiz6jpHLUnhnOELJEZ2G4uOM130_provenance.
- NP64833.RA_VuU03G83QCvGhaaspXhiz6jpHLUnhnOELJEZ2G4uOM130_assertion evidence source_evidence_literature NP64833.RA_VuU03G83QCvGhaaspXhiz6jpHLUnhnOELJEZ2G4uOM130_provenance.
- NP64833.RA_VuU03G83QCvGhaaspXhiz6jpHLUnhnOELJEZ2G4uOM130_assertion SIO_000772 17204961 NP64833.RA_VuU03G83QCvGhaaspXhiz6jpHLUnhnOELJEZ2G4uOM130_provenance.
- NP64833.RA_VuU03G83QCvGhaaspXhiz6jpHLUnhnOELJEZ2G4uOM130_assertion wasDerivedFrom gad-20150221 NP64833.RA_VuU03G83QCvGhaaspXhiz6jpHLUnhnOELJEZ2G4uOM130_provenance.
- NP64833.RA_VuU03G83QCvGhaaspXhiz6jpHLUnhnOELJEZ2G4uOM130_assertion wasGeneratedBy ECO_0000203 NP64833.RA_VuU03G83QCvGhaaspXhiz6jpHLUnhnOELJEZ2G4uOM130_provenance.
- gad-20150221 importedOn "2015-02-21" NP64833.RA_VuU03G83QCvGhaaspXhiz6jpHLUnhnOELJEZ2G4uOM130_provenance.