Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1097408.RAx0ZXQNZEr2va9Pb28GNobPf33e4Kw8rpc28zhi3QuDw130_assertion> ?p ?o ?g. }
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- NP1097408.RAx0ZXQNZEr2va9Pb28GNobPf33e4Kw8rpc28zhi3QuDw130_assertion type Assertion NP1097408.RAx0ZXQNZEr2va9Pb28GNobPf33e4Kw8rpc28zhi3QuDw130_head.
- NP1097408.RAx0ZXQNZEr2va9Pb28GNobPf33e4Kw8rpc28zhi3QuDw130_assertion wasGeneratedBy ECO_0000203 NP1097408.RAx0ZXQNZEr2va9Pb28GNobPf33e4Kw8rpc28zhi3QuDw130_provenance.
- NP1097408.RAx0ZXQNZEr2va9Pb28GNobPf33e4Kw8rpc28zhi3QuDw130_assertion wasDerivedFrom befree-2016 NP1097408.RAx0ZXQNZEr2va9Pb28GNobPf33e4Kw8rpc28zhi3QuDw130_provenance.
- NP1097408.RAx0ZXQNZEr2va9Pb28GNobPf33e4Kw8rpc28zhi3QuDw130_assertion SIO_000772 23892095 NP1097408.RAx0ZXQNZEr2va9Pb28GNobPf33e4Kw8rpc28zhi3QuDw130_provenance.
- NP1097408.RAx0ZXQNZEr2va9Pb28GNobPf33e4Kw8rpc28zhi3QuDw130_assertion evidence source_evidence_literature NP1097408.RAx0ZXQNZEr2va9Pb28GNobPf33e4Kw8rpc28zhi3QuDw130_provenance.
- NP1097408.RAx0ZXQNZEr2va9Pb28GNobPf33e4Kw8rpc28zhi3QuDw130_assertion description "[Cystic fibrosis (CF) is an autosomal recessive disease caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene, which encodes an epithelial anion channel.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1097408.RAx0ZXQNZEr2va9Pb28GNobPf33e4Kw8rpc28zhi3QuDw130_provenance.