Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP194288.RAXwcpjZXztVlQ8--SeRwdDwQcaEDZtZkXJqhM4GSUc0Y130_assertion> ?p ?o ?g. }
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- NP194288.RAXwcpjZXztVlQ8--SeRwdDwQcaEDZtZkXJqhM4GSUc0Y130_assertion type Assertion NP194288.RAXwcpjZXztVlQ8--SeRwdDwQcaEDZtZkXJqhM4GSUc0Y130_head.
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- NP194288.RAXwcpjZXztVlQ8--SeRwdDwQcaEDZtZkXJqhM4GSUc0Y130_assertion SIO_000772 18306312 NP194288.RAXwcpjZXztVlQ8--SeRwdDwQcaEDZtZkXJqhM4GSUc0Y130_provenance.
- NP194288.RAXwcpjZXztVlQ8--SeRwdDwQcaEDZtZkXJqhM4GSUc0Y130_assertion evidence source_evidence_literature NP194288.RAXwcpjZXztVlQ8--SeRwdDwQcaEDZtZkXJqhM4GSUc0Y130_provenance.
- NP194288.RAXwcpjZXztVlQ8--SeRwdDwQcaEDZtZkXJqhM4GSUc0Y130_assertion description "[results predict a major impact of the CFTR missense variants analyzed, except p.R75Q, on the cystic fibrosis phenotype and highlight the importance of the CFTR N-terminus on channel physiology]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP194288.RAXwcpjZXztVlQ8--SeRwdDwQcaEDZtZkXJqhM4GSUc0Y130_provenance.