Matches in Nanopublications for { ?s ?p "[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."@en ?g. }
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- 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." provenance.
- NP311166.RASx2Zd39XscRRXEHbbBOisTTptWI5_TSTDzhSMKS3OJ8130_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." NP311166.RASx2Zd39XscRRXEHbbBOisTTptWI5_TSTDzhSMKS3OJ8130_provenance.
- 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.