RDF/XMLNTriplesTurtleShow queryShare
SubjectPredicateObject
http://purl.uniprot.org/citations/28264986http://purl.uniprot.org/core/author"Majewski J."xsd:string
http://purl.uniprot.org/citations/28264986http://purl.uniprot.org/core/author"Chodirker B."xsd:string
http://purl.uniprot.org/citations/28264986http://purl.uniprot.org/core/group"Canadian Rare Diseases: Models & Mechanisms Network,"xsd:string
http://purl.uniprot.org/citations/28264986http://purl.uniprot.org/core/title"A truncating mutation in CEP55 is the likely cause of MARCH, a novel syndrome affecting neuronal mitosis."xsd:string
http://purl.uniprot.org/uniprot/#_Q53EZ4-citation-28264986http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/28264986
http://purl.uniprot.org/uniprot/#_Q502I3-citation-28264986http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/28264986
http://purl.uniprot.org/citations/28264986http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/28264986
http://purl.uniprot.org/citations/28264986http://purl.uniprot.org/core/author"Katsanis N."xsd:string
http://purl.uniprot.org/uniprot/Q502I3#attribution-AD26A54C353EA479460FF88DE44000C5http://purl.uniprot.org/core/sourcehttp://purl.uniprot.org/citations/28264986
http://purl.uniprot.org/uniprot/Q53EZ4#attribution-BC162F593D859E5F3994DB1A986FE791http://purl.uniprot.org/core/sourcehttp://purl.uniprot.org/citations/28264986
http://purl.uniprot.org/citations/28264986http://purl.uniprot.org/core/author"Philippe J."xsd:string
http://purl.uniprot.org/uniprot/Q502I3#attribution-329AFBB667FFD9A319192811F15D135Bhttp://purl.uniprot.org/core/sourcehttp://purl.uniprot.org/citations/28264986
http://purl.uniprot.org/citations/28264986http://purl.uniprot.org/core/volume"54"xsd:string
http://purl.uniprot.org/citations/28264986http://purl.uniprot.org/core/author"Liu Y.P."xsd:string
http://purl.uniprot.org/citations/28264986http://purl.uniprot.org/core/author"Simard L."xsd:string
http://purl.uniprot.org/citations/28264986http://purl.uniprot.org/core/author"Davis E.E."xsd:string
http://purl.uniprot.org/citations/28264986http://purl.uniprot.org/core/author"Fahiminiya S."xsd:string
http://purl.uniprot.org/citations/28264986http://purl.uniprot.org/core/pages"490-501"xsd:string
http://purl.uniprot.org/citations/28264986http://purl.uniprot.org/core/author"Hegele R."xsd:string
http://purl.uniprot.org/citations/28264986http://purl.uniprot.org/core/author"Brown E.L."xsd:string
http://purl.uniprot.org/citations/28264986http://purl.uniprot.org/core/author"Russell C."xsd:string
http://purl.uniprot.org/citations/28264986http://purl.uniprot.org/core/date"2017"xsd:gYear
http://purl.uniprot.org/citations/28264986http://purl.uniprot.org/core/author"Gunn C.S."xsd:string
http://purl.uniprot.org/citations/28264986http://purl.uniprot.org/core/group"FORGE Canada Consortium"xsd:string
http://purl.uniprot.org/citations/28264986http://purl.uniprot.org/core/name"J. Med. Genet."xsd:string