RDF/XMLNTriplesTurtleShow queryShare
SubjectPredicateObject
http://purl.uniprot.org/uniprot/#_R9UNY3-mappedCitation-17220209http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/17220209
http://purl.uniprot.org/citations/17220209http://purl.org/dc/terms/identifier"doi:10.1136/jmg.2006.046904"xsd:string
http://purl.uniprot.org/uniprot/#_V9GYK6-mappedCitation-17220209http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/17220209
http://purl.uniprot.org/citations/17220209http://purl.uniprot.org/core/author"Desir J."xsd:string
http://purl.uniprot.org/citations/17220209http://purl.uniprot.org/core/author"David K.L."xsd:string
http://purl.uniprot.org/uniprot/#_R9UQ62-mappedCitation-17220209http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/17220209
http://purl.uniprot.org/uniprot/Q8NBS3#attribution-1AC91C4E9F687566B39BF93F59D915B8http://purl.uniprot.org/core/sourcehttp://purl.uniprot.org/citations/17220209
http://purl.uniprot.org/citations/17220209http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/17220209http://purl.uniprot.org/core/name"J. Med. Genet."xsd:string
http://purl.uniprot.org/citations/17220209http://purl.uniprot.org/core/author"Deconinck H."xsd:string
http://purl.uniprot.org/citations/17220209http://purl.uniprot.org/core/date"2007"xsd:gYear
http://purl.uniprot.org/uniprot/R9UQ62http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/17220209
http://purl.uniprot.org/citations/17220209http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/17220209
http://purl.uniprot.org/uniprot/#_R9UQ64-mappedCitation-17220209http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/17220209
http://purl.uniprot.org/citations/17220209http://purl.uniprot.org/core/author"Van Regemorter N."xsd:string
http://purl.uniprot.org/citations/17220209http://purl.uniprot.org/core/author"Moya G."xsd:string
http://purl.uniprot.org/citations/17220209http://purl.uniprot.org/core/title"Borate transporter SLC4A11 mutations cause both Harboyan syndrome and non-syndromic corneal endothelial dystrophy."xsd:string
http://purl.uniprot.org/citations/17220209http://purl.uniprot.org/core/pages"322-326"xsd:string
http://purl.uniprot.org/citations/17220209http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/17220209
http://purl.uniprot.org/citations/17220209http://purl.uniprot.org/core/author"Abramowicz M.J."xsd:string
http://purl.uniprot.org/uniprot/#_R9UMG9-mappedCitation-17220209http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/17220209
http://purl.uniprot.org/citations/17220209http://purl.uniprot.org/core/volume"44"xsd:string
http://purl.uniprot.org/citations/17220209http://purl.uniprot.org/core/author"Meire F.M."xsd:string
http://purl.uniprot.org/uniprot/Q8NBS3http://purl.uniprot.org/core/citationhttp://purl.uniprot.org/citations/17220209
http://purl.uniprot.org/uniprot/#_R9UQ67-mappedCitation-17220209http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/17220209