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http://purl.uniprot.org/uniprot/#_P51608-citation-12966522http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/12966522
http://purl.uniprot.org/citations/12966522http://purl.uniprot.org/core/title"Rett syndrome in a 47,XXX patient with a de novo MECP2 mutation."xsd:string
http://purl.uniprot.org/citations/12966522http://purl.org/dc/terms/identifier"doi:10.1002/ajmg.a.20320"xsd:string
http://purl.uniprot.org/citations/12966522http://purl.uniprot.org/core/volume"122"xsd:string
http://purl.uniprot.org/citations/12966522http://purl.uniprot.org/core/author"Hammer S."xsd:string
http://purl.uniprot.org/citations/12966522http://purl.uniprot.org/core/name"Am. J. Med. Genet. A"xsd:string
http://purl.uniprot.org/citations/12966522http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/12966522
http://purl.uniprot.org/citations/12966522http://purl.uniprot.org/core/pages"223-226"xsd:string
http://purl.uniprot.org/uniprot/P51608http://purl.uniprot.org/core/citationhttp://purl.uniprot.org/citations/12966522
http://purl.uniprot.org/citations/12966522http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/12966522
http://purl.uniprot.org/citations/12966522http://purl.uniprot.org/core/author"Dorrani N."xsd:string
http://purl.uniprot.org/citations/12966522http://purl.uniprot.org/core/date"2003"xsd:gYear
http://purl.uniprot.org/citations/12966522http://purl.uniprot.org/core/author"Schanen N.C."xsd:string
http://purl.uniprot.org/citations/12966522http://purl.uniprot.org/core/author"Hartiala J."xsd:string
http://purl.uniprot.org/uniprot/P51608#attribution-CCBADA88D92F39A5EB632C6A1E250FE9http://purl.uniprot.org/core/sourcehttp://purl.uniprot.org/citations/12966522
http://purl.uniprot.org/citations/12966522http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/12966522http://purl.uniprot.org/core/author"Stein S."xsd:string