http://purl.uniprot.org/uniprot/#_P04156-citation-8909447 | http://www.w3.org/1999/02/22-rdf-syntax-ns#object | http://purl.uniprot.org/citations/8909447 |
http://purl.uniprot.org/citations/8909447 | http://www.w3.org/2004/02/skos/core#exactMatch | http://purl.uniprot.org/pubmed/8909447 |
http://purl.uniprot.org/uniprot/P04156#attribution-F55DEFCFB7C5F4F9551856DD1F67B4AE | http://purl.uniprot.org/core/source | http://purl.uniprot.org/citations/8909447 |
http://purl.uniprot.org/citations/8909447 | http://www.w3.org/1999/02/22-rdf-syntax-ns#type | http://purl.uniprot.org/core/Journal_Citation |
http://purl.uniprot.org/citations/8909447 | http://xmlns.com/foaf/0.1/primaryTopicOf | https://pubmed.ncbi.nlm.nih.gov/8909447 |
http://purl.uniprot.org/uniprot/P04156 | http://purl.uniprot.org/core/citation | http://purl.uniprot.org/citations/8909447 |
http://purl.uniprot.org/citations/8909447 | http://purl.org/dc/terms/identifier | "doi:10.1212/wnl.47.5.1305"xsd:string |
http://purl.uniprot.org/citations/8909447 | http://purl.uniprot.org/core/author | "Iannicola C."xsd:string |
http://purl.uniprot.org/citations/8909447 | http://purl.uniprot.org/core/author | "Prusiner S.B."xsd:string |
http://purl.uniprot.org/citations/8909447 | http://purl.uniprot.org/core/author | "Myers R.M."xsd:string |
http://purl.uniprot.org/citations/8909447 | http://purl.uniprot.org/core/author | "Mastrianni J.A."xsd:string |
http://purl.uniprot.org/citations/8909447 | http://purl.uniprot.org/core/date | "1996"xsd:gYear |
http://purl.uniprot.org/citations/8909447 | http://purl.uniprot.org/core/volume | "47"xsd:string |
http://purl.uniprot.org/citations/8909447 | http://purl.uniprot.org/core/pages | "1305-1312"xsd:string |
http://purl.uniprot.org/citations/8909447 | http://purl.uniprot.org/core/name | "Neurology"xsd:string |
http://purl.uniprot.org/citations/8909447 | http://purl.uniprot.org/core/author | "Dearmond S."xsd:string |
http://purl.uniprot.org/citations/8909447 | http://purl.uniprot.org/core/title | "Mutation of the prion protein gene at codon 208 in familial Creutzfeldt-Jakob disease."xsd:string |