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http://purl.uniprot.org/citations/23812912http://purl.uniprot.org/core/author"Brockmann K."xsd:string
http://purl.uniprot.org/uniprot/#_B4DYN7-mappedCitation-23812912http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/23812912
http://purl.uniprot.org/citations/23812912http://purl.uniprot.org/core/author"Edvardson S."xsd:string
http://purl.uniprot.org/citations/23812912http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/23812912
http://purl.uniprot.org/citations/23812912http://purl.uniprot.org/core/date"2013"xsd:gYear
http://purl.uniprot.org/citations/23812912http://purl.uniprot.org/core/author"Gaertner J."xsd:string
http://purl.uniprot.org/citations/23812912http://purl.uniprot.org/core/author"Henneke M."xsd:string
http://purl.uniprot.org/citations/23812912http://purl.org/dc/terms/identifier"doi:10.1136/jmedgenet-2013-101752"xsd:string
http://purl.uniprot.org/uniprot/B4DYN7http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/23812912
http://purl.uniprot.org/citations/23812912http://purl.uniprot.org/core/author"Elpeleg O."xsd:string
http://purl.uniprot.org/citations/23812912http://purl.uniprot.org/core/title"West syndrome, microcephaly, grey matter heterotopia and hypoplasia of corpus callosum due to a novel ARFGEF2 mutation."xsd:string
http://purl.uniprot.org/citations/23812912http://purl.uniprot.org/core/volume"50"xsd:string
http://purl.uniprot.org/citations/23812912http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/uniprot/B3KMT7http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/23812912
http://purl.uniprot.org/citations/23812912http://purl.uniprot.org/core/author"Banne E."xsd:string
http://purl.uniprot.org/citations/23812912http://purl.uniprot.org/core/pages"772-775"xsd:string
http://purl.uniprot.org/citations/23812912http://purl.uniprot.org/core/author"Atawneh O."xsd:string
http://purl.uniprot.org/uniprot/Q59FR3http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/23812912
http://purl.uniprot.org/uniprot/Q9Y6D5#attribution-A5A77150265895476B5633C87DCE9769http://purl.uniprot.org/core/sourcehttp://purl.uniprot.org/citations/23812912
http://purl.uniprot.org/uniprot/#_Q59FR3-mappedCitation-23812912http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/23812912
http://purl.uniprot.org/citations/23812912http://purl.uniprot.org/core/name"J. Med. Genet."xsd:string
http://purl.uniprot.org/uniprot/Q9Y6D5http://purl.uniprot.org/core/citationhttp://purl.uniprot.org/citations/23812912
http://purl.uniprot.org/uniprot/#_Q86TH5-mappedCitation-23812912http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/23812912
http://purl.uniprot.org/uniprot/#_B3KMT7-mappedCitation-23812912http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/23812912
http://purl.uniprot.org/citations/23812912http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/23812912