Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP64758.RAAxiK_UMFhC_XWwx1RerQvqGvEdDqGfqFRwEwPOxNnlA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP64758.RAAxiK_UMFhC_XWwx1RerQvqGvEdDqGfqFRwEwPOxNnlA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP64758.RAAxiK_UMFhC_XWwx1RerQvqGvEdDqGfqFRwEwPOxNnlA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP64758.RAAxiK_UMFhC_XWwx1RerQvqGvEdDqGfqFRwEwPOxNnlA130_provenance.
- NP64758.RAAxiK_UMFhC_XWwx1RerQvqGvEdDqGfqFRwEwPOxNnlA130_assertion description "[These mutations were not detected among 100 healthy control subjects, suggesting a possible pathogenetic role of ACT gene defects in a subset of patients with COPD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP64758.RAAxiK_UMFhC_XWwx1RerQvqGvEdDqGfqFRwEwPOxNnlA130_provenance.
- NP64758.RAAxiK_UMFhC_XWwx1RerQvqGvEdDqGfqFRwEwPOxNnlA130_assertion evidence source_evidence_literature NP64758.RAAxiK_UMFhC_XWwx1RerQvqGvEdDqGfqFRwEwPOxNnlA130_provenance.
- NP64758.RAAxiK_UMFhC_XWwx1RerQvqGvEdDqGfqFRwEwPOxNnlA130_assertion SIO_000772 8244391 NP64758.RAAxiK_UMFhC_XWwx1RerQvqGvEdDqGfqFRwEwPOxNnlA130_provenance.
- NP64758.RAAxiK_UMFhC_XWwx1RerQvqGvEdDqGfqFRwEwPOxNnlA130_assertion wasDerivedFrom gad-20150221 NP64758.RAAxiK_UMFhC_XWwx1RerQvqGvEdDqGfqFRwEwPOxNnlA130_provenance.
- NP64758.RAAxiK_UMFhC_XWwx1RerQvqGvEdDqGfqFRwEwPOxNnlA130_assertion wasGeneratedBy ECO_0000203 NP64758.RAAxiK_UMFhC_XWwx1RerQvqGvEdDqGfqFRwEwPOxNnlA130_provenance.
- gad-20150221 importedOn "2015-02-21" NP64758.RAAxiK_UMFhC_XWwx1RerQvqGvEdDqGfqFRwEwPOxNnlA130_provenance.