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- NP1311662.RAiLZPR-rXn0WneE2EYh471vCGPfzeGtnW1uur7VaMgsM130_assertion type Assertion NP1311662.RAiLZPR-rXn0WneE2EYh471vCGPfzeGtnW1uur7VaMgsM130_head.
- NP1311662.RAiLZPR-rXn0WneE2EYh471vCGPfzeGtnW1uur7VaMgsM130_assertion description "[The pulmonary disease reflects mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene, and associated abnormal epithelial ion transport, including defective cAMP-mediated (CFTR) Cl- secretion and an accelerated rate of basal Na+ transport.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1311662.RAiLZPR-rXn0WneE2EYh471vCGPfzeGtnW1uur7VaMgsM130_provenance.
- NP1311662.RAiLZPR-rXn0WneE2EYh471vCGPfzeGtnW1uur7VaMgsM130_assertion evidence source_evidence_literature NP1311662.RAiLZPR-rXn0WneE2EYh471vCGPfzeGtnW1uur7VaMgsM130_provenance.
- NP1311662.RAiLZPR-rXn0WneE2EYh471vCGPfzeGtnW1uur7VaMgsM130_assertion SIO_000772 7542031 NP1311662.RAiLZPR-rXn0WneE2EYh471vCGPfzeGtnW1uur7VaMgsM130_provenance.
- NP1311662.RAiLZPR-rXn0WneE2EYh471vCGPfzeGtnW1uur7VaMgsM130_assertion wasDerivedFrom befree-2016 NP1311662.RAiLZPR-rXn0WneE2EYh471vCGPfzeGtnW1uur7VaMgsM130_provenance.
- NP1311662.RAiLZPR-rXn0WneE2EYh471vCGPfzeGtnW1uur7VaMgsM130_assertion wasGeneratedBy ECO_0000203 NP1311662.RAiLZPR-rXn0WneE2EYh471vCGPfzeGtnW1uur7VaMgsM130_provenance.