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http://purl.uniprot.org/citations/1574115http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/1574115http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/1574115http://www.w3.org/2000/01/rdf-schema#comment"Fanconi's anaemia is a rare autosomal recessive disorder characterized by progressive pancytopaenia and a cellular hypersensitivity to DNA crosslinking agents. Four genetic complementation groups have been identified so far, and here we use a functional complementation method to clone complementary DNAs that correct the defect of group C cells. The cDNAs encode alternatively processed transcripts of a new gene, designated FACC, which is mutated in group C patients. The predicted FACC polypeptide does not contain any motifs common to other proteins and so represents a new gene involved in the cellular response to DNA damage."xsd:string
http://purl.uniprot.org/citations/1574115http://purl.org/dc/terms/identifier"doi:10.1038/356763a0"xsd:string
http://purl.uniprot.org/citations/1574115http://purl.org/dc/terms/identifier"doi:10.1038/356763a0"xsd:string
http://purl.uniprot.org/citations/1574115http://purl.uniprot.org/core/author"Buchwald M."xsd:string
http://purl.uniprot.org/citations/1574115http://purl.uniprot.org/core/author"Buchwald M."xsd:string
http://purl.uniprot.org/citations/1574115http://purl.uniprot.org/core/author"Strathdee C.A."xsd:string
http://purl.uniprot.org/citations/1574115http://purl.uniprot.org/core/author"Strathdee C.A."xsd:string
http://purl.uniprot.org/citations/1574115http://purl.uniprot.org/core/author"Gavish H."xsd:string
http://purl.uniprot.org/citations/1574115http://purl.uniprot.org/core/author"Gavish H."xsd:string
http://purl.uniprot.org/citations/1574115http://purl.uniprot.org/core/author"Shannon W.R."xsd:string
http://purl.uniprot.org/citations/1574115http://purl.uniprot.org/core/author"Shannon W.R."xsd:string
http://purl.uniprot.org/citations/1574115http://purl.uniprot.org/core/date"1992"xsd:gYear
http://purl.uniprot.org/citations/1574115http://purl.uniprot.org/core/date"1992"xsd:gYear
http://purl.uniprot.org/citations/1574115http://purl.uniprot.org/core/name"Nature"xsd:string
http://purl.uniprot.org/citations/1574115http://purl.uniprot.org/core/name"Nature"xsd:string
http://purl.uniprot.org/citations/1574115http://purl.uniprot.org/core/pages"763-767"xsd:string
http://purl.uniprot.org/citations/1574115http://purl.uniprot.org/core/pages"763-767"xsd:string
http://purl.uniprot.org/citations/1574115http://purl.uniprot.org/core/title"Cloning of cDNAs for Fanconi's anaemia by functional complementation."xsd:string
http://purl.uniprot.org/citations/1574115http://purl.uniprot.org/core/title"Cloning of cDNAs for Fanconi's anaemia by functional complementation."xsd:string
http://purl.uniprot.org/citations/1574115http://purl.uniprot.org/core/volume"356"xsd:string
http://purl.uniprot.org/citations/1574115http://purl.uniprot.org/core/volume"356"xsd:string
http://purl.uniprot.org/citations/1574115http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/1574115
http://purl.uniprot.org/citations/1574115http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/1574115