RDF/XMLNTriplesTurtleShow queryShare
SubjectPredicateObject
http://purl.uniprot.org/citations/18593874http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/18593874http://www.w3.org/2000/01/rdf-schema#comment"Dyskeratosis congenita (DC) is a rare syndrome, characterized by cutaneous abnormalities and premature death caused by bone marrow failure. In this issue of Genes & Development, Hockemeyer and colleagues (pp. 1773-1785) report a new mouse model that reconstitutes key features of DC. Disease phenotypes are generated by a POT1b deletion in a telomerase-deficient background that accelerates the shortening of telomeres by degradation."xsd:string
http://purl.uniprot.org/citations/18593874http://purl.org/dc/terms/identifier"doi:10.1101/gad.1695808"xsd:string
http://purl.uniprot.org/citations/18593874http://purl.uniprot.org/core/author"Autexier C."xsd:string
http://purl.uniprot.org/citations/18593874http://purl.uniprot.org/core/date"2008"xsd:gYear
http://purl.uniprot.org/citations/18593874http://purl.uniprot.org/core/name"Genes Dev"xsd:string
http://purl.uniprot.org/citations/18593874http://purl.uniprot.org/core/pages"1731-1736"xsd:string
http://purl.uniprot.org/citations/18593874http://purl.uniprot.org/core/title"POT of gold: modeling dyskeratosis congenita in the mouse."xsd:string
http://purl.uniprot.org/citations/18593874http://purl.uniprot.org/core/volume"22"xsd:string
http://purl.uniprot.org/citations/18593874http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/18593874
http://purl.uniprot.org/citations/18593874http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/18593874
http://purl.uniprot.org/uniprot/#_A0A3B2WCG4-mappedCitation-18593874http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/18593874
http://purl.uniprot.org/uniprot/#_A0A3B2WCZ2-mappedCitation-18593874http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/18593874
http://purl.uniprot.org/uniprot/#_A2RSK4-mappedCitation-18593874http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/18593874
http://purl.uniprot.org/uniprot/#_H7BX60-mappedCitation-18593874http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/18593874
http://purl.uniprot.org/uniprot/#_P24699-mappedCitation-18593874http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/18593874
http://purl.uniprot.org/uniprot/#_Q3TNS5-mappedCitation-18593874http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/18593874
http://purl.uniprot.org/uniprot/#_Q8VHZ2-mappedCitation-18593874http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/18593874
http://purl.uniprot.org/uniprot/A0A3B2WCG4http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/18593874
http://purl.uniprot.org/uniprot/Q8VHZ2http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/18593874
http://purl.uniprot.org/uniprot/A0A3B2WCZ2http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/18593874
http://purl.uniprot.org/uniprot/Q3TNS5http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/18593874
http://purl.uniprot.org/uniprot/A2RSK4http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/18593874
http://purl.uniprot.org/uniprot/P24699http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/18593874
http://purl.uniprot.org/uniprot/H7BX60http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/18593874