RDF/XMLNTriplesTurtleShow queryShare
SubjectPredicateObject
http://purl.uniprot.org/citations/37308312http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/37308312http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/37308312http://www.w3.org/2000/01/rdf-schema#comment"A Loss-of-function variant in ZNF808 is associated with non-syndromic neonatal diabetes in a consanguineous family with three affected siblings."xsd:string
http://purl.uniprot.org/citations/37308312http://purl.org/dc/terms/identifier"doi:10.1111/cge.14389"xsd:string
http://purl.uniprot.org/citations/37308312http://purl.org/dc/terms/identifier"doi:10.1111/cge.14389"xsd:string
http://purl.uniprot.org/citations/37308312http://purl.uniprot.org/core/author"Almontashiri N.A.M."xsd:string
http://purl.uniprot.org/citations/37308312http://purl.uniprot.org/core/author"Almontashiri N.A.M."xsd:string
http://purl.uniprot.org/citations/37308312http://purl.uniprot.org/core/author"Alharby E."xsd:string
http://purl.uniprot.org/citations/37308312http://purl.uniprot.org/core/author"Alharby E."xsd:string
http://purl.uniprot.org/citations/37308312http://purl.uniprot.org/core/author"Al-Falki Y.H."xsd:string
http://purl.uniprot.org/citations/37308312http://purl.uniprot.org/core/author"Al-Falki Y.H."xsd:string
http://purl.uniprot.org/citations/37308312http://purl.uniprot.org/core/author"Al-Qahtani S.M."xsd:string
http://purl.uniprot.org/citations/37308312http://purl.uniprot.org/core/author"Al-Qahtani S.M."xsd:string
http://purl.uniprot.org/citations/37308312http://purl.uniprot.org/core/author"Albulym O.M."xsd:string
http://purl.uniprot.org/citations/37308312http://purl.uniprot.org/core/author"Albulym O.M."xsd:string
http://purl.uniprot.org/citations/37308312http://purl.uniprot.org/core/author"Alqahtani M.A."xsd:string
http://purl.uniprot.org/citations/37308312http://purl.uniprot.org/core/author"Alqahtani M.A."xsd:string
http://purl.uniprot.org/citations/37308312http://purl.uniprot.org/core/date"2023"xsd:gYear
http://purl.uniprot.org/citations/37308312http://purl.uniprot.org/core/date"2023"xsd:gYear
http://purl.uniprot.org/citations/37308312http://purl.uniprot.org/core/name"Clin. Genet."xsd:string
http://purl.uniprot.org/citations/37308312http://purl.uniprot.org/core/name"Clin. Genet."xsd:string
http://purl.uniprot.org/citations/37308312http://purl.uniprot.org/core/pages"497-498"xsd:string
http://purl.uniprot.org/citations/37308312http://purl.uniprot.org/core/pages"497-498"xsd:string
http://purl.uniprot.org/citations/37308312http://purl.uniprot.org/core/title"Biallelic loss of function variant in ZNF808 is associated with non-syndromic neonatal diabetes."xsd:string
http://purl.uniprot.org/citations/37308312http://purl.uniprot.org/core/title"Biallelic loss of function variant in ZNF808 is associated with non-syndromic neonatal diabetes."xsd:string