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SubjectPredicateObject
http://purl.uniprot.org/uniprot/E7D7Y0http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/22052856
http://purl.uniprot.org/citations/22052856http://purl.uniprot.org/core/name"Am. J. Med. Genet. A"xsd:string
http://purl.uniprot.org/uniprot/#_E7D7Y0-mappedCitation-22052856http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/22052856
http://purl.uniprot.org/uniprot/J3QL32http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/22052856
http://purl.uniprot.org/uniprot/#_Q8TBX0-mappedCitation-22052856http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/22052856
http://purl.uniprot.org/citations/22052856http://purl.uniprot.org/core/author"Jian Y.R."xsd:string
http://purl.uniprot.org/citations/22052856http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/22052856http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/22052856
http://purl.uniprot.org/uniprot/#_A0A1B2JLU7-mappedCitation-22052856http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/22052856
http://purl.uniprot.org/citations/22052856http://purl.uniprot.org/core/author"Huang Y.W."xsd:string
http://purl.uniprot.org/citations/22052856http://purl.uniprot.org/core/author"Yeung C.Y."xsd:string
http://purl.uniprot.org/uniprot/#_P32322-citation-22052856http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/22052856
http://purl.uniprot.org/citations/22052856http://purl.uniprot.org/core/pages"3095-3099"xsd:string
http://purl.uniprot.org/citations/22052856http://purl.uniprot.org/core/author"Ho C.S."xsd:string
http://purl.uniprot.org/uniprot/P32322#attribution-9253FBDBD2466254D087E1138F4B92F8http://purl.uniprot.org/core/sourcehttp://purl.uniprot.org/citations/22052856
http://purl.uniprot.org/citations/22052856http://purl.uniprot.org/core/date"2011"xsd:gYear
http://purl.uniprot.org/citations/22052856http://purl.uniprot.org/core/title"Compound heterozygous mutations in PYCR1 further expand the phenotypic spectrum of De Barsy syndrome."xsd:string
http://purl.uniprot.org/uniprot/D6QXZ5http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/22052856
http://purl.uniprot.org/uniprot/#_E7D7X9-mappedCitation-22052856http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/22052856
http://purl.uniprot.org/uniprot/A0A1B2JLU7http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/22052856
http://purl.uniprot.org/uniprot/Q8TBX0http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/22052856
http://purl.uniprot.org/citations/22052856http://purl.uniprot.org/core/author"Chiang M.F."xsd:string
http://purl.uniprot.org/citations/22052856http://purl.uniprot.org/core/author"Huang Z.D."xsd:string
http://purl.uniprot.org/citations/22052856http://purl.uniprot.org/core/author"Wu T.Y."xsd:string
http://purl.uniprot.org/citations/22052856http://purl.uniprot.org/core/author"Chang J.H."xsd:string