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http://purl.uniprot.org/citations/11030761 | http://purl.uniprot.org/core/author | "Goodwin B."xsd:string |
http://purl.uniprot.org/citations/11030761 | http://purl.uniprot.org/core/date | "2000"xsd:gYear |
http://purl.uniprot.org/citations/11030761 | http://purl.uniprot.org/core/author | "Hopwood B."xsd:string |
http://purl.uniprot.org/citations/11030761 | http://xmlns.com/foaf/0.1/primaryTopicOf | https://pubmed.ncbi.nlm.nih.gov/11030761 |
http://purl.uniprot.org/citations/11030761 | http://purl.uniprot.org/core/author | "Haan E."xsd:string |
http://purl.uniprot.org/citations/11030761 | http://purl.uniprot.org/core/author | "Cox L.L."xsd:string |
http://purl.uniprot.org/citations/11030761 | http://www.w3.org/1999/02/22-rdf-syntax-ns#type | http://purl.uniprot.org/core/Journal_Citation |
http://purl.uniprot.org/citations/11030761 | http://purl.uniprot.org/core/name | "Hum. Mol. Genet."xsd:string |
http://purl.uniprot.org/citations/11030761 | http://purl.uniprot.org/core/title | "New mutations in MID1 provide support for loss of function as the cause of X-linked Opitz syndrome."xsd:string |
http://purl.uniprot.org/citations/11030761 | http://www.w3.org/2004/02/skos/core#exactMatch | http://purl.uniprot.org/pubmed/11030761 |
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http://purl.uniprot.org/citations/11030761 | http://purl.uniprot.org/core/author | "Allen L.R."xsd:string |
http://purl.uniprot.org/citations/11030761 | http://purl.org/dc/terms/identifier | "doi:10.1093/hmg/9.17.2553"xsd:string |
http://purl.uniprot.org/citations/11030761 | http://purl.uniprot.org/core/pages | "2553-2562"xsd:string |
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http://purl.uniprot.org/citations/11030761 | http://purl.uniprot.org/core/author | "Suthers G.K."xsd:string |
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