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http://purl.uniprot.org/citations/15060124http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/15060124http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/15060124http://purl.org/dc/terms/identifier"doi:10.1136/jmg.2003.011890"xsd:string
http://purl.uniprot.org/citations/15060124http://purl.org/dc/terms/identifier"doi:10.1136/jmg.2003.011890"xsd:string
http://purl.uniprot.org/citations/15060124http://purl.uniprot.org/core/author"Tarpey P."xsd:string
http://purl.uniprot.org/citations/15060124http://purl.uniprot.org/core/author"Tarpey P."xsd:string
http://purl.uniprot.org/citations/15060124http://purl.uniprot.org/core/author"Baralle D."xsd:string
http://purl.uniprot.org/citations/15060124http://purl.uniprot.org/core/author"Baralle D."xsd:string
http://purl.uniprot.org/citations/15060124http://purl.uniprot.org/core/author"Whittaker J."xsd:string
http://purl.uniprot.org/citations/15060124http://purl.uniprot.org/core/author"Whittaker J."xsd:string
http://purl.uniprot.org/citations/15060124http://purl.uniprot.org/core/author"Bobrow M."xsd:string
http://purl.uniprot.org/citations/15060124http://purl.uniprot.org/core/author"Bobrow M."xsd:string
http://purl.uniprot.org/citations/15060124http://purl.uniprot.org/core/author"Mattocks C."xsd:string
http://purl.uniprot.org/citations/15060124http://purl.uniprot.org/core/author"Mattocks C."xsd:string
http://purl.uniprot.org/citations/15060124http://purl.uniprot.org/core/author"ffrench-Constant C."xsd:string
http://purl.uniprot.org/citations/15060124http://purl.uniprot.org/core/author"ffrench-Constant C."xsd:string
http://purl.uniprot.org/citations/15060124http://purl.uniprot.org/core/date"2004"xsd:gYear
http://purl.uniprot.org/citations/15060124http://purl.uniprot.org/core/date"2004"xsd:gYear
http://purl.uniprot.org/citations/15060124http://purl.uniprot.org/core/name"J. Med. Genet."xsd:string
http://purl.uniprot.org/citations/15060124http://purl.uniprot.org/core/name"J. Med. Genet."xsd:string
http://purl.uniprot.org/citations/15060124http://purl.uniprot.org/core/pages"E48"xsd:string
http://purl.uniprot.org/citations/15060124http://purl.uniprot.org/core/pages"E48"xsd:string
http://purl.uniprot.org/citations/15060124http://purl.uniprot.org/core/title"Automated comparative sequence analysis identifies mutations in 89% of NF1 patients and confirms a mutation cluster in exons 11-17 distinct from the GAP related domain."xsd:string
http://purl.uniprot.org/citations/15060124http://purl.uniprot.org/core/title"Automated comparative sequence analysis identifies mutations in 89% of NF1 patients and confirms a mutation cluster in exons 11-17 distinct from the GAP related domain."xsd:string
http://purl.uniprot.org/citations/15060124http://purl.uniprot.org/core/volume"41"xsd:string