Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1090703.RA8BLrRc12hrzeA5s9lyC4lrP1ZZm6RX8Is8lYzBIyGIc130_assertion> ?p ?o ?g. }
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- NP1090703.RA8BLrRc12hrzeA5s9lyC4lrP1ZZm6RX8Is8lYzBIyGIc130_assertion type Assertion NP1090703.RA8BLrRc12hrzeA5s9lyC4lrP1ZZm6RX8Is8lYzBIyGIc130_head.
- NP1090703.RA8BLrRc12hrzeA5s9lyC4lrP1ZZm6RX8Is8lYzBIyGIc130_assertion description "[Cystic fibrosis (CF) is caused by loss-of-function mutations in the CF transmembrane conductance regulator (CFTR) protein, a cAMP-regulated anion channel expressed primarily at the apical plasma membrane of secretory epithelia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1090703.RA8BLrRc12hrzeA5s9lyC4lrP1ZZm6RX8Is8lYzBIyGIc130_provenance.
- NP1090703.RA8BLrRc12hrzeA5s9lyC4lrP1ZZm6RX8Is8lYzBIyGIc130_assertion evidence source_evidence_literature NP1090703.RA8BLrRc12hrzeA5s9lyC4lrP1ZZm6RX8Is8lYzBIyGIc130_provenance.
- NP1090703.RA8BLrRc12hrzeA5s9lyC4lrP1ZZm6RX8Is8lYzBIyGIc130_assertion SIO_000772 23818513 NP1090703.RA8BLrRc12hrzeA5s9lyC4lrP1ZZm6RX8Is8lYzBIyGIc130_provenance.
- NP1090703.RA8BLrRc12hrzeA5s9lyC4lrP1ZZm6RX8Is8lYzBIyGIc130_assertion wasDerivedFrom befree-2016 NP1090703.RA8BLrRc12hrzeA5s9lyC4lrP1ZZm6RX8Is8lYzBIyGIc130_provenance.
- NP1090703.RA8BLrRc12hrzeA5s9lyC4lrP1ZZm6RX8Is8lYzBIyGIc130_assertion wasGeneratedBy ECO_0000203 NP1090703.RA8BLrRc12hrzeA5s9lyC4lrP1ZZm6RX8Is8lYzBIyGIc130_provenance.