{"?xml":{"@version":"1.0"},"edm:RDF":{"@xmlns:dc":"http://purl.org/dc/elements/1.1/","@xmlns:edm":"http://www.europeana.eu/schemas/edm/","@xmlns:wgs84_pos":"http://www.w3.org/2003/01/geo/wgs84_pos","@xmlns:foaf":"http://xmlns.com/foaf/0.1/","@xmlns:rdaGr2":"http://rdvocab.info/ElementsGr2","@xmlns:oai":"http://www.openarchives.org/OAI/2.0/","@xmlns:owl":"http://www.w3.org/2002/07/owl#","@xmlns:rdf":"http://www.w3.org/1999/02/22-rdf-syntax-ns#","@xmlns:ore":"http://www.openarchives.org/ore/terms/","@xmlns:skos":"http://www.w3.org/2004/02/skos/core#","@xmlns:dcterms":"http://purl.org/dc/terms/","edm:WebResource":[{"@rdf:about":"http://www.dlib.si/stream/URN:NBN:SI:doc-PR88FX5R/06883165-ea02-4736-9228-93ba684c7e86/PDF","dcterms:extent":"690 KB"},{"@rdf:about":"http://www.dlib.si/stream/URN:NBN:SI:doc-PR88FX5R/e1881f92-bb94-4523-85c9-84e0d2371b82/TEXT","dcterms:extent":"17 KB"}],"edm:TimeSpan":{"@rdf:about":"1992-2025","edm:begin":{"@xml:lang":"en","#text":"1992"},"edm:end":{"@xml:lang":"en","#text":"2025"}},"edm:ProvidedCHO":{"@rdf:about":"URN:NBN:SI:doc-PR88FX5R","dcterms:isPartOf":[{"@rdf:resource":"https://www.dlib.si/details/URN:NBN:SI:SPR-WQVGMCSC"},{"@xml:lang":"sl","#text":"Acta dermatovenerologica Alpina, Pannonica et Adriatica"}],"dcterms:issued":"2003","dc:creator":["Centurión, Santiago A.","Schwartz, Robert A."],"dc:format":[{"@xml:lang":"sl","#text":"številka:1"},{"@xml:lang":"sl","#text":"letnik:12"},{"@xml:lang":"sl","#text":"str. 32-36"}],"dc:identifier":["ISSN:1318-4458","COBISSID:16238553","URN:URN:NBN:SI:doc-PR88FX5R"],"dc:language":"en","dc:publisher":{"@xml:lang":"sl","#text":"Slovene Welding Society"},"dc:subject":[{"@xml:lang":"en","#text":"Albinism, Oculocutaneous"},{"@xml:lang":"sl","#text":"Albinizem okulokutani"},{"@xml:lang":"en","#text":"Angelman Syndrome"},{"@xml:lang":"sl","#text":"Angelmanov sindrom"},{"@xml:lang":"sl","#text":"Chediak-Hagashijev sindrom"},{"@xml:lang":"en","#text":"Chediak-Higashi Syndrome"},{"@xml:lang":"sl","#text":"dermatologija"},{"@xml:lang":"en","#text":"Diagnosis"},{"@xml:lang":"en","#text":"diagnostika"},{"@xml:lang":"sl","#text":"etiologija"},{"@xml:lang":"sl","#text":"kožne bolezni"},{"@xml:lang":"en","#text":"Pathology"},{"@xml:lang":"en","#text":"Prader-Willi Syndrome"},{"@xml:lang":"sl","#text":"Prader-Willijev sindrom"},{"@xml:lang":"en","#text":"Therapy"}],"dcterms:temporal":{"@rdf:resource":"1992-2025"},"dc:title":{"@xml:lang":"sl","#text":"Oculocutaneous albinism type 2|"},"dc:description":{"@xml:lang":"sl","#text":"Oculocutaneous albinism represents a group of inherited skin disorders characterized by a generalized reduction of cutaneous, ocular, and pilar pigmentation from the time of birth. Oculocutaneous albinism types I and II are the most common, with several other types described. A defect in the melanin synthesis pathway, resulting in reduced formation of melanin, is responsible for oculocutaneous albinism. The etiology, clinical manifestations, diagnosis, and management are discussed"},"edm:type":"TEXT","dc:type":[{"@xml:lang":"sl","#text":"znanstveno časopisje"},{"@xml:lang":"en","#text":"journals"},{"@rdf:resource":"http://www.wikidata.org/entity/Q361785"}]},"ore:Aggregation":{"@rdf:about":"http://www.dlib.si/?URN=URN:NBN:SI:doc-PR88FX5R","edm:aggregatedCHO":{"@rdf:resource":"URN:NBN:SI:doc-PR88FX5R"},"edm:isShownBy":{"@rdf:resource":"http://www.dlib.si/stream/URN:NBN:SI:doc-PR88FX5R/06883165-ea02-4736-9228-93ba684c7e86/PDF"},"edm:rights":{"@rdf:resource":"http://rightsstatements.org/vocab/InC/1.0/"},"edm:provider":"Slovenian National E-content Aggregator","edm:intermediateProvider":{"@xml:lang":"en","#text":"National and University Library of Slovenia"},"edm:dataProvider":{"@xml:lang":"sl","#text":"Združenje slovenskih dermatovenerologov"},"edm:object":{"@rdf:resource":"http://www.dlib.si/streamdb/URN:NBN:SI:doc-PR88FX5R/maxi/edm"},"edm:isShownAt":{"@rdf:resource":"http://www.dlib.si/details/URN:NBN:SI:doc-PR88FX5R"}}}}