Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1312210.RA_SZnb9sDFRelR6Y-cT6HefGaGVdxwXIvUNkWjED53cY130_assertion> ?p ?o ?g. }
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- NP1312210.RA_SZnb9sDFRelR6Y-cT6HefGaGVdxwXIvUNkWjED53cY130_assertion type Assertion NP1312210.RA_SZnb9sDFRelR6Y-cT6HefGaGVdxwXIvUNkWjED53cY130_head.
- NP1312210.RA_SZnb9sDFRelR6Y-cT6HefGaGVdxwXIvUNkWjED53cY130_assertion description "[Congenital bilateral absence of the vas deferens (CBAVD) in some patients arises from mutations within the cystic fibrosis (CF) transmembrane regulator (CFTR) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1312210.RA_SZnb9sDFRelR6Y-cT6HefGaGVdxwXIvUNkWjED53cY130_provenance.
- NP1312210.RA_SZnb9sDFRelR6Y-cT6HefGaGVdxwXIvUNkWjED53cY130_assertion evidence source_evidence_literature NP1312210.RA_SZnb9sDFRelR6Y-cT6HefGaGVdxwXIvUNkWjED53cY130_provenance.
- NP1312210.RA_SZnb9sDFRelR6Y-cT6HefGaGVdxwXIvUNkWjED53cY130_assertion SIO_000772 7551394 NP1312210.RA_SZnb9sDFRelR6Y-cT6HefGaGVdxwXIvUNkWjED53cY130_provenance.
- NP1312210.RA_SZnb9sDFRelR6Y-cT6HefGaGVdxwXIvUNkWjED53cY130_assertion wasDerivedFrom befree-2016 NP1312210.RA_SZnb9sDFRelR6Y-cT6HefGaGVdxwXIvUNkWjED53cY130_provenance.
- NP1312210.RA_SZnb9sDFRelR6Y-cT6HefGaGVdxwXIvUNkWjED53cY130_assertion wasGeneratedBy ECO_0000203 NP1312210.RA_SZnb9sDFRelR6Y-cT6HefGaGVdxwXIvUNkWjED53cY130_provenance.