http://purl.uniprot.org/citations/12949970 | http://purl.org/dc/terms/identifier | "doi:10.1002/ajmg.a.20260"xsd:string |
http://purl.uniprot.org/uniprot/P23760#attribution-7A062D54888F48578EA35F03DB610166 | http://purl.uniprot.org/core/source | http://purl.uniprot.org/citations/12949970 |
http://purl.uniprot.org/citations/12949970 | http://www.w3.org/2004/02/skos/core#exactMatch | http://purl.uniprot.org/pubmed/12949970 |
http://purl.uniprot.org/citations/12949970 | http://www.w3.org/1999/02/22-rdf-syntax-ns#type | http://purl.uniprot.org/core/Journal_Citation |
http://purl.uniprot.org/citations/12949970 | http://purl.uniprot.org/core/date | "2003"xsd:gYear |
http://purl.uniprot.org/citations/12949970 | http://purl.uniprot.org/core/author | "Uyguner O."xsd:string |
http://purl.uniprot.org/citations/12949970 | http://purl.uniprot.org/core/volume | "122"xsd:string |
http://purl.uniprot.org/citations/12949970 | http://purl.uniprot.org/core/author | "Ghanbari A."xsd:string |
http://purl.uniprot.org/citations/12949970 | http://purl.uniprot.org/core/name | "Am. J. Med. Genet. A"xsd:string |
http://purl.uniprot.org/uniprot/P23760 | http://purl.uniprot.org/core/citation | http://purl.uniprot.org/citations/12949970 |
http://purl.uniprot.org/citations/12949970 | http://xmlns.com/foaf/0.1/primaryTopicOf | https://pubmed.ncbi.nlm.nih.gov/12949970 |
http://purl.uniprot.org/citations/12949970 | http://purl.uniprot.org/core/author | "Yuksel-Apak M."xsd:string |
http://purl.uniprot.org/uniprot/#_P23760-citation-12949970 | http://www.w3.org/1999/02/22-rdf-syntax-ns#object | http://purl.uniprot.org/citations/12949970 |
http://purl.uniprot.org/citations/12949970 | http://purl.uniprot.org/core/pages | "42-45"xsd:string |
http://purl.uniprot.org/citations/12949970 | http://purl.uniprot.org/core/author | "Emiroglu M."xsd:string |
http://purl.uniprot.org/citations/12949970 | http://purl.uniprot.org/core/author | "Kayserili H."xsd:string |
http://purl.uniprot.org/citations/12949970 | http://purl.uniprot.org/core/title | "Homozygous and heterozygous inheritance of PAX3 mutations causes different types of Waardenburg syndrome."xsd:string |
http://purl.uniprot.org/citations/12949970 | http://purl.uniprot.org/core/author | "Wollnik B."xsd:string |
http://purl.uniprot.org/citations/12949970 | http://purl.uniprot.org/core/author | "Tukel T."xsd:string |