RDF/XMLNTriplesTurtleShow queryShare
SubjectPredicateObject
http://purl.uniprot.org/citations/7505694http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/7505694http://purl.uniprot.org/core/date"1993"xsd:gYear
http://purl.uniprot.org/citations/7505694http://purl.uniprot.org/core/author"Casals T."xsd:string
http://purl.uniprot.org/citations/7505694http://purl.uniprot.org/core/author"Chillon M."xsd:string
http://purl.uniprot.org/citations/7505694http://purl.uniprot.org/core/pages"1741-1742"xsd:string
http://purl.uniprot.org/citations/7505694http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/7505694
http://purl.uniprot.org/uniprot/P13569http://purl.uniprot.org/core/citationhttp://purl.uniprot.org/citations/7505694
http://purl.uniprot.org/citations/7505694http://purl.uniprot.org/core/name"Hum. Mol. Genet."xsd:string
http://purl.uniprot.org/citations/7505694http://purl.uniprot.org/core/author"Estivill X."xsd:string
http://purl.uniprot.org/citations/7505694http://purl.org/dc/terms/identifier"doi:10.1093/hmg/2.10.1741"xsd:string
http://purl.uniprot.org/uniprot/P13569#attribution-1E3E80DC8C728E62CE484F714A9DE82Fhttp://purl.uniprot.org/core/sourcehttp://purl.uniprot.org/citations/7505694
http://purl.uniprot.org/citations/7505694http://purl.uniprot.org/core/author"Nunes V."xsd:string
http://purl.uniprot.org/citations/7505694http://purl.uniprot.org/core/volume"2"xsd:string
http://purl.uniprot.org/citations/7505694http://purl.uniprot.org/core/author"Gimenez J."xsd:string
http://purl.uniprot.org/citations/7505694http://purl.uniprot.org/core/author"Ruiz E.P."xsd:string
http://purl.uniprot.org/citations/7505694http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/7505694
http://purl.uniprot.org/uniprot/#_P13569-citation-7505694http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/7505694
http://purl.uniprot.org/citations/7505694http://purl.uniprot.org/core/title"Identification of a new missense mutation (P205S) in the first transmembrane domain of the CFTR gene associated with a mild cystic fibrosis phenotype."xsd:string