Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP294425.RABuJBG-57XYErRJqM7UfAFK-sgUxoKUPRyJbk8nYchrs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP294425.RABuJBG-57XYErRJqM7UfAFK-sgUxoKUPRyJbk8nYchrs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP294425.RABuJBG-57XYErRJqM7UfAFK-sgUxoKUPRyJbk8nYchrs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP294425.RABuJBG-57XYErRJqM7UfAFK-sgUxoKUPRyJbk8nYchrs130_provenance.
- befree-2016 importedOn "2016-02-19" NP294425.RABuJBG-57XYErRJqM7UfAFK-sgUxoKUPRyJbk8nYchrs130_provenance.
- NP294425.RABuJBG-57XYErRJqM7UfAFK-sgUxoKUPRyJbk8nYchrs130_assertion wasGeneratedBy ECO_0000203 NP294425.RABuJBG-57XYErRJqM7UfAFK-sgUxoKUPRyJbk8nYchrs130_provenance.
- NP294425.RABuJBG-57XYErRJqM7UfAFK-sgUxoKUPRyJbk8nYchrs130_assertion wasDerivedFrom befree-2016 NP294425.RABuJBG-57XYErRJqM7UfAFK-sgUxoKUPRyJbk8nYchrs130_provenance.
- NP294425.RABuJBG-57XYErRJqM7UfAFK-sgUxoKUPRyJbk8nYchrs130_assertion SIO_000772 10977777 NP294425.RABuJBG-57XYErRJqM7UfAFK-sgUxoKUPRyJbk8nYchrs130_provenance.
- NP294425.RABuJBG-57XYErRJqM7UfAFK-sgUxoKUPRyJbk8nYchrs130_assertion evidence source_evidence_literature NP294425.RABuJBG-57XYErRJqM7UfAFK-sgUxoKUPRyJbk8nYchrs130_provenance.
- NP294425.RABuJBG-57XYErRJqM7UfAFK-sgUxoKUPRyJbk8nYchrs130_assertion description "[We performed an association study of patients with IgA nephropathy and matching control subjects to test whether the G38A polymorphism in the uteroglobin gene, the C2093T polymorphism in the megsin gene, or the angiotensin-converting enzyme (ACE) insertion/deletion polymorphism is associated with IgA nephropathy or rate of disease progression in patients with IgA nephropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP294425.RABuJBG-57XYErRJqM7UfAFK-sgUxoKUPRyJbk8nYchrs130_provenance.