http://purl.uniprot.org/citations/10206685 | http://purl.uniprot.org/core/author | "Beauville L."xsd:string |
http://purl.uniprot.org/uniprot/Q14191 | http://purl.uniprot.org/core/citation | http://purl.uniprot.org/citations/10206685 |
http://purl.uniprot.org/citations/10206685 | http://purl.uniprot.org/core/author | "Bay J.-O."xsd:string |
http://purl.uniprot.org/citations/10206685 | http://purl.uniprot.org/core/volume | "11"xsd:string |
http://purl.uniprot.org/citations/10206685 | http://www.w3.org/1999/02/22-rdf-syntax-ns#type | http://purl.uniprot.org/core/Journal_Citation |
http://purl.uniprot.org/uniprot/Q14191#attribution-F59C4EA0E9A5EEF27A5665E93B308096 | http://purl.uniprot.org/core/source | http://purl.uniprot.org/citations/10206685 |
http://purl.uniprot.org/citations/10206685 | http://purl.uniprot.org/core/date | "1998"xsd:gYear |
http://purl.uniprot.org/citations/10206685 | http://purl.uniprot.org/core/author | "Vidal V."xsd:string |
http://purl.uniprot.org/citations/10206685 | http://www.w3.org/2004/02/skos/core#exactMatch | http://purl.uniprot.org/pubmed/10206685 |
http://purl.uniprot.org/citations/10206685 | http://xmlns.com/foaf/0.1/primaryTopicOf | https://pubmed.ncbi.nlm.nih.gov/10206685 |
http://purl.uniprot.org/citations/10206685 | http://purl.uniprot.org/core/author | "Champomier F."xsd:string |
http://purl.uniprot.org/citations/10206685 | http://purl.uniprot.org/core/author | "Grancho M."xsd:string |
http://purl.uniprot.org/citations/10206685 | http://purl.uniprot.org/core/author | "Ferrara M."xsd:string |
http://purl.uniprot.org/citations/10206685 | http://purl.uniprot.org/core/author | "Glowaczower C."xsd:string |
http://purl.uniprot.org/citations/10206685 | http://purl.uniprot.org/core/author | "Bignon Y.-J."xsd:string |
http://purl.uniprot.org/uniprot/#_Q14191-citation-10206685 | http://www.w3.org/1999/02/22-rdf-syntax-ns#object | http://purl.uniprot.org/citations/10206685 |
http://purl.uniprot.org/citations/10206685 | http://purl.uniprot.org/core/title | "The 1396del A mutation and a missense mutation or a rare polymorphism of the WRN gene detected in a French Werner family with a severe phenotype and a case of an unusual vulvar cancer."xsd:string |
http://purl.uniprot.org/citations/10206685 | http://purl.uniprot.org/core/pages | "413-414"xsd:string |
http://purl.uniprot.org/citations/10206685 | http://purl.uniprot.org/core/author | "Lemery D."xsd:string |
http://purl.uniprot.org/citations/10206685 | http://purl.uniprot.org/core/name | "Hum. Mutat."xsd:string |