Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP11685.RAGlofJr8pRTyUQ6bxXXoL0MRApVkZg-lQVFrMoT9Eirw130_assertion> ?p ?o ?g. }
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- NP11685.RAGlofJr8pRTyUQ6bxXXoL0MRApVkZg-lQVFrMoT9Eirw130_assertion type Assertion NP11685.RAGlofJr8pRTyUQ6bxXXoL0MRApVkZg-lQVFrMoT9Eirw130_head.
- NP11685.RAGlofJr8pRTyUQ6bxXXoL0MRApVkZg-lQVFrMoT9Eirw130_assertion wasGeneratedBy ECO_0000218 NP11685.RAGlofJr8pRTyUQ6bxXXoL0MRApVkZg-lQVFrMoT9Eirw130_provenance.
- NP11685.RAGlofJr8pRTyUQ6bxXXoL0MRApVkZg-lQVFrMoT9Eirw130_assertion wasDerivedFrom ctd_human-20130708 NP11685.RAGlofJr8pRTyUQ6bxXXoL0MRApVkZg-lQVFrMoT9Eirw130_provenance.
- NP11685.RAGlofJr8pRTyUQ6bxXXoL0MRApVkZg-lQVFrMoT9Eirw130_assertion SIO_000772 18230692 NP11685.RAGlofJr8pRTyUQ6bxXXoL0MRApVkZg-lQVFrMoT9Eirw130_provenance.
- NP11685.RAGlofJr8pRTyUQ6bxXXoL0MRApVkZg-lQVFrMoT9Eirw130_assertion evidence source_evidence_curated NP11685.RAGlofJr8pRTyUQ6bxXXoL0MRApVkZg-lQVFrMoT9Eirw130_provenance.
- NP11685.RAGlofJr8pRTyUQ6bxXXoL0MRApVkZg-lQVFrMoT9Eirw130_assertion description "[The most common mutation (F508del) causing cystic fibrosis (CF) results in misfolding of the CF transmembrane conductance regulator (CFTR), leading to its degradation via the proteasome pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP11685.RAGlofJr8pRTyUQ6bxXXoL0MRApVkZg-lQVFrMoT9Eirw130_provenance.