Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1175795.RA380_JkigSXkhwQqsmB3ePiqE-uPFBWtADZQ6Tc9v7sY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1175795.RA380_JkigSXkhwQqsmB3ePiqE-uPFBWtADZQ6Tc9v7sY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1175795.RA380_JkigSXkhwQqsmB3ePiqE-uPFBWtADZQ6Tc9v7sY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1175795.RA380_JkigSXkhwQqsmB3ePiqE-uPFBWtADZQ6Tc9v7sY130_provenance.
- NP1175795.RA380_JkigSXkhwQqsmB3ePiqE-uPFBWtADZQ6Tc9v7sY130_assertion description "[CFTR (cystic fibrosis transmembrane conductance regulator) is a cAMP-regulated Cl(-) channel in the apical membrane of epithelium that contributes to salt and water secretion onto the luminal surface of airways, thereby ensuring that secreted mucus is sufficiently hydrated for movement along the epithelial surface.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1175795.RA380_JkigSXkhwQqsmB3ePiqE-uPFBWtADZQ6Tc9v7sY130_provenance.
- NP1175795.RA380_JkigSXkhwQqsmB3ePiqE-uPFBWtADZQ6Tc9v7sY130_assertion evidence source_evidence_literature NP1175795.RA380_JkigSXkhwQqsmB3ePiqE-uPFBWtADZQ6Tc9v7sY130_provenance.
- NP1175795.RA380_JkigSXkhwQqsmB3ePiqE-uPFBWtADZQ6Tc9v7sY130_assertion SIO_000772 24755862 NP1175795.RA380_JkigSXkhwQqsmB3ePiqE-uPFBWtADZQ6Tc9v7sY130_provenance.
- NP1175795.RA380_JkigSXkhwQqsmB3ePiqE-uPFBWtADZQ6Tc9v7sY130_assertion wasDerivedFrom befree-2016 NP1175795.RA380_JkigSXkhwQqsmB3ePiqE-uPFBWtADZQ6Tc9v7sY130_provenance.
- NP1175795.RA380_JkigSXkhwQqsmB3ePiqE-uPFBWtADZQ6Tc9v7sY130_assertion wasGeneratedBy ECO_0000203 NP1175795.RA380_JkigSXkhwQqsmB3ePiqE-uPFBWtADZQ6Tc9v7sY130_provenance.
- befree-2016 importedOn "2016-02-19" NP1175795.RA380_JkigSXkhwQqsmB3ePiqE-uPFBWtADZQ6Tc9v7sY130_provenance.