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| http://purl.uniprot.org/citations/16094673 | http://purl.uniprot.org/core/author | "Muschol N."xsd:string |
| http://purl.uniprot.org/citations/16094673 | http://purl.uniprot.org/core/author | "Tiede S."xsd:string |
| http://purl.uniprot.org/citations/16094673 | http://purl.uniprot.org/core/pages | "235-240"xsd:string |
| http://purl.uniprot.org/citations/16094673 | http://purl.uniprot.org/core/date | "2005"xsd:gYear |
| http://purl.uniprot.org/citations/16094673 | http://www.w3.org/2004/02/skos/core#exactMatch | http://purl.uniprot.org/pubmed/16094673 |
| http://purl.uniprot.org/citations/16094673 | http://purl.org/dc/terms/identifier | "doi:10.1002/ajmg.a.30868"xsd:string |
| http://purl.uniprot.org/uniprot/#_Q3T906-citation-16094673 | http://www.w3.org/1999/02/22-rdf-syntax-ns#object | http://purl.uniprot.org/citations/16094673 |
| http://purl.uniprot.org/citations/16094673 | http://purl.uniprot.org/core/author | "Cantz M."xsd:string |
| http://purl.uniprot.org/citations/16094673 | http://purl.uniprot.org/core/author | "Reutter G."xsd:string |
| http://purl.uniprot.org/citations/16094673 | http://xmlns.com/foaf/0.1/primaryTopicOf | https://pubmed.ncbi.nlm.nih.gov/16094673 |
| http://purl.uniprot.org/citations/16094673 | http://purl.uniprot.org/core/volume | "137"xsd:string |
| http://purl.uniprot.org/citations/16094673 | http://purl.uniprot.org/core/author | "Braulke T."xsd:string |
| http://purl.uniprot.org/citations/16094673 | http://purl.uniprot.org/core/author | "Ullrich K."xsd:string |
| http://purl.uniprot.org/uniprot/Q3T906 | http://purl.uniprot.org/core/citation | http://purl.uniprot.org/citations/16094673 |
| http://purl.uniprot.org/uniprot/Q3T906#attribution-2E3252BCB59456D6CE02B44B7E266304 | http://purl.uniprot.org/core/source | http://purl.uniprot.org/citations/16094673 |
| http://purl.uniprot.org/citations/16094673 | http://purl.uniprot.org/core/name | "Am. J. Med. Genet. A"xsd:string |
| http://purl.uniprot.org/citations/16094673 | http://purl.uniprot.org/core/title | "Missense mutations in N-acetylglucosamine-1-phosphotransferase alpha/beta subunit gene in a patient with mucolipidosis III and a mild clinical phenotype."xsd:string |