http://purl.uniprot.org/uniprot/#_P15289-citation-10751093 | http://www.w3.org/1999/02/22-rdf-syntax-ns#object | http://purl.uniprot.org/citations/10751093 |
http://purl.uniprot.org/uniprot/P15289#attribution-E20E4FB831093EDB5579701F9CE4E87C | http://purl.uniprot.org/core/source | http://purl.uniprot.org/citations/10751093 |
http://purl.uniprot.org/citations/10751093 | http://www.w3.org/1999/02/22-rdf-syntax-ns#type | http://purl.uniprot.org/core/Journal_Citation |
http://purl.uniprot.org/uniprot/P15289 | http://purl.uniprot.org/core/citation | http://purl.uniprot.org/citations/10751093 |
http://purl.uniprot.org/citations/10751093 | http://xmlns.com/foaf/0.1/primaryTopicOf | https://pubmed.ncbi.nlm.nih.gov/10751093 |
http://purl.uniprot.org/citations/10751093 | http://purl.uniprot.org/core/volume | "91"xsd:string |
http://purl.uniprot.org/citations/10751093 | http://purl.uniprot.org/core/author | "Zlotogora J."xsd:string |
http://purl.uniprot.org/citations/10751093 | http://purl.org/dc/terms/identifier | "doi:10.1002/(sici)1096-8628(20000306)91:1<68::aid-ajmg13>3.0.co;2-g"xsd:string |
http://purl.uniprot.org/citations/10751093 | http://purl.uniprot.org/core/pages | "68-73"xsd:string |
http://purl.uniprot.org/citations/10751093 | http://purl.uniprot.org/core/author | "Kafert S."xsd:string |
http://purl.uniprot.org/citations/10751093 | http://purl.uniprot.org/core/author | "Schestag F."xsd:string |
http://purl.uniprot.org/citations/10751093 | http://purl.uniprot.org/core/author | "Baumann N."xsd:string |
http://purl.uniprot.org/citations/10751093 | http://purl.uniprot.org/core/author | "Polten A."xsd:string |
http://purl.uniprot.org/citations/10751093 | http://purl.uniprot.org/core/name | "Am. J. Med. Genet."xsd:string |
http://purl.uniprot.org/citations/10751093 | http://www.w3.org/2004/02/skos/core#exactMatch | http://purl.uniprot.org/pubmed/10751093 |
http://purl.uniprot.org/citations/10751093 | http://purl.uniprot.org/core/author | "Penzien J."xsd:string |
http://purl.uniprot.org/citations/10751093 | http://purl.uniprot.org/core/title | "Characterization of four arylsulfatase A missense mutations G86D, Y201C, D255H, and E312D causing metachromatic leukodystrophy."xsd:string |
http://purl.uniprot.org/citations/10751093 | http://purl.uniprot.org/core/author | "Hermann S."xsd:string |
http://purl.uniprot.org/citations/10751093 | http://purl.uniprot.org/core/author | "Gieselmann V."xsd:string |
http://purl.uniprot.org/citations/10751093 | http://purl.uniprot.org/core/date | "2000"xsd:gYear |