Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP538504.RAuCFLFhbrO3JoSTJrlIAI4FvGRL2Zdp1mHmokgMyzmH4130_assertion> ?p ?o ?g. }
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- NP538504.RAuCFLFhbrO3JoSTJrlIAI4FvGRL2Zdp1mHmokgMyzmH4130_assertion type Assertion NP538504.RAuCFLFhbrO3JoSTJrlIAI4FvGRL2Zdp1mHmokgMyzmH4130_head.
- NP538504.RAuCFLFhbrO3JoSTJrlIAI4FvGRL2Zdp1mHmokgMyzmH4130_assertion description "[The 5T allele of the polyT tract located within intron 8 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene is a variant that in trans with a severe CFTR mutation can result in normal phenotype, congenital bilateral absence of vas deferens (CBAVD), or mild cystic fibrosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP538504.RAuCFLFhbrO3JoSTJrlIAI4FvGRL2Zdp1mHmokgMyzmH4130_provenance.
- NP538504.RAuCFLFhbrO3JoSTJrlIAI4FvGRL2Zdp1mHmokgMyzmH4130_assertion evidence source_evidence_literature NP538504.RAuCFLFhbrO3JoSTJrlIAI4FvGRL2Zdp1mHmokgMyzmH4130_provenance.
- NP538504.RAuCFLFhbrO3JoSTJrlIAI4FvGRL2Zdp1mHmokgMyzmH4130_assertion SIO_000772 17234733 NP538504.RAuCFLFhbrO3JoSTJrlIAI4FvGRL2Zdp1mHmokgMyzmH4130_provenance.
- NP538504.RAuCFLFhbrO3JoSTJrlIAI4FvGRL2Zdp1mHmokgMyzmH4130_assertion wasDerivedFrom befree-20140225 NP538504.RAuCFLFhbrO3JoSTJrlIAI4FvGRL2Zdp1mHmokgMyzmH4130_provenance.
- NP538504.RAuCFLFhbrO3JoSTJrlIAI4FvGRL2Zdp1mHmokgMyzmH4130_assertion wasGeneratedBy ECO_0000203 NP538504.RAuCFLFhbrO3JoSTJrlIAI4FvGRL2Zdp1mHmokgMyzmH4130_provenance.