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SubjectPredicateObject
http://purl.uniprot.org/citations/16380922http://purl.uniprot.org/core/name"Am. J. Hum. Genet."xsd:string
http://purl.uniprot.org/uniprot/Q56NI9#attribution-7694EAC8C30A1FB1C4DCBDFFDA783064http://purl.uniprot.org/core/sourcehttp://purl.uniprot.org/citations/16380922
http://purl.uniprot.org/citations/16380922http://purl.org/dc/terms/identifier"doi:10.1086/498695"xsd:string
http://purl.uniprot.org/citations/16380922http://purl.uniprot.org/core/date"2005"xsd:gYear
http://purl.uniprot.org/citations/16380922http://purl.uniprot.org/core/author"Francke U."xsd:string
http://purl.uniprot.org/citations/16380922http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/16380922
http://purl.uniprot.org/citations/16380922http://purl.uniprot.org/core/pages"1117-1128"xsd:string
http://purl.uniprot.org/uniprot/#_Q56NI9-citation-16380922http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/16380922
http://purl.uniprot.org/citations/16380922http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/16380922
http://purl.uniprot.org/citations/16380922http://purl.uniprot.org/core/volume"77"xsd:string
http://purl.uniprot.org/uniprot/Q56NI9http://purl.uniprot.org/core/citationhttp://purl.uniprot.org/citations/16380922
http://purl.uniprot.org/citations/16380922http://purl.uniprot.org/core/author"Oviedo A."xsd:string
http://purl.uniprot.org/citations/16380922http://purl.uniprot.org/core/title"Inactivating mutations in ESCO2 cause SC phocomelia and Roberts syndrome: no phenotype-genotype correlation."xsd:string
http://purl.uniprot.org/citations/16380922http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/16380922http://purl.uniprot.org/core/author"Schuele B."xsd:string
http://purl.uniprot.org/citations/16380922http://purl.uniprot.org/core/author"Johnston K."xsd:string
http://purl.uniprot.org/citations/16380922http://purl.uniprot.org/core/author"Pai S."xsd:string