<?xml version="1.0"?><rdf: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-KA13XBER/a8092d27-ce70-44c2-adad-827e27f74820/PDF"><dcterms:extent>79 KB</dcterms:extent></edm:WebResource><edm:WebResource rdf:about="http://www.dlib.si/stream/URN:NBN:SI:DOC-KA13XBER/c57b01a3-666e-40b9-8584-575e5b0041d7/TEXT"><dcterms:extent>42 KB</dcterms:extent></edm:WebResource><edm:TimeSpan rdf:about="1994-2025"><edm:begin xml:lang="en">1994</edm:begin><edm:end xml:lang="en">2025</edm:end></edm:TimeSpan><edm:ProvidedCHO rdf:about="URN:NBN:SI:DOC-KA13XBER"><dcterms:isPartOf rdf:resource="https://www.dlib.si/details/URN:NBN:SI:spr-46R7GGHL" /><dcterms:issued>1999</dcterms:issued><dc:creator>Kores-Plesničar, Blanka</dc:creator><dc:creator>Velikonja, Ingrid</dc:creator><dc:format xml:lang="sl">številka:1</dc:format><dc:format xml:lang="sl">letnik:38</dc:format><dc:format xml:lang="sl">str. 117-129</dc:format><dc:identifier>ISSN:0025-8121</dc:identifier><dc:identifier>COBISSID:10161113</dc:identifier><dc:identifier>URN:URN:NBN:SI:doc-KA13XBER</dc:identifier><dc:language>sl</dc:language><dc:publisher xml:lang="sl">Medicinski razgledi</dc:publisher><dcterms:isPartOf xml:lang="sl">Medicinski razgledi</dcterms:isPartOf><dc:subject xml:lang="en">Chromosome abnormalities</dc:subject><dc:subject xml:lang="en">Chromosomes, human, pair 11</dc:subject><dc:subject xml:lang="en">Chromosomes, human, pair 22</dc:subject><dc:subject xml:lang="en">Chromosomes, human, pair 5</dc:subject><dc:subject xml:lang="sl">dedovanje</dc:subject><dc:subject xml:lang="en">Genetics</dc:subject><dc:subject xml:lang="sl">genetika</dc:subject><dc:subject xml:lang="sl">geni</dc:subject><dc:subject xml:lang="en">Pedigree</dc:subject><dc:subject xml:lang="en">Schizophrenia</dc:subject><dc:subject xml:lang="sl">shizofrenija</dc:subject><dc:subject xml:lang="en">X chromosome</dc:subject><dc:subject rdf:resource="http://www.wikidata.org/entity/Q840741" /><dcterms:temporal rdf:resource="1994-2025" /><dc:title xml:lang="sl">Genetika shizofrenije| Genetics of schizophrenia|</dc:title><dc:description xml:lang="sl">The authors give a brief description of schizophrenia based on the establishedinternational criteria, and discuss its epidemiology and aetiology.They present family, twin and adoption studies wich have reinforced the role of genetic factors in the aetiology of schizophrenia. Next they discuss various inheritance patterns, the hypothesis of the site of a single gene locus for schizophrenia and role of non-genetics factors. Recent studies aimed at detecting and localizing the dominant gene linked to schizophrenia ona locus of chromosome 6 seem most promising, yet evi- dence is accumulating that the mode of inheritance is either polygenic (caused by many genes exerting slight effects), or oligogenic (caused by a few genes exerting moderate effects), with an important role being played by environmental factors. Modern genetic methods will certainly improve our understanding of the aetiology and development of schizophrenia in the foreseeable future</dc:description><dc:description xml:lang="sl">Avtorici najprej kratko predstavita shizofrenske motnje po veljavnih mednarodnih klasifikacijskih merilih, njihovo epidemiologijo in izvor. Opisaneso raziskave rodovnikov velikih družin, dvojčkov in posvojencev, ki potrjujejo pomembno vlogo genetskega dejavnika pri razvoju shizofrenije. Omenjeni so različni načini njenega genetskega prenosa, hipoteze o lokalizaciji lokusa za shizofrenijo kot tudi pomen in vloga negenetskih dejavnikov. Pri odkrivanju dominantnega gena za shizofrenijo v zadnjem času največ obetajo proučevanja sumljivih lokusov na kromosomu 6, čeprav se vse bolj uveljavlja prepričanje o poligenskem (nekaj genov z zmernim vplivom) oziroma oligogenskem (več genov z manjšim vplivom) načinu dedovanja, seveda obupoštevanju raznovrstnih dejavnikov okolja. Sodobne genetske metode bodo v prihodnosti nedvomno omogočile boljše poznavanje in razumevanje na- stanka, prenosa in razvoja shizofrenije</dc:description><edm:type>TEXT</edm:type><dc:type xml:lang="sl">znanstveno časopisje</dc:type><dc:type xml:lang="en">journals</dc:type><dc:type rdf:resource="http://www.wikidata.org/entity/Q361785" /></edm:ProvidedCHO><ore:Aggregation rdf:about="http://www.dlib.si/?URN=URN:NBN:SI:DOC-KA13XBER"><edm:aggregatedCHO rdf:resource="URN:NBN:SI:DOC-KA13XBER" /><edm:isShownBy rdf:resource="http://www.dlib.si/stream/URN:NBN:SI:DOC-KA13XBER/a8092d27-ce70-44c2-adad-827e27f74820/PDF" /><edm:rights rdf:resource="http://rightsstatements.org/vocab/InC/1.0/" /><edm:provider>Slovenian National E-content Aggregator</edm:provider><edm:intermediateProvider xml:lang="en">National and University Library of Slovenia</edm:intermediateProvider><edm:dataProvider xml:lang="sl">Društvo Medicinski razgledi</edm:dataProvider><edm:object rdf:resource="http://www.dlib.si/streamdb/URN:NBN:SI:DOC-KA13XBER/maxi/edm" /><edm:isShownAt rdf:resource="http://www.dlib.si/details/URN:NBN:SI:DOC-KA13XBER" /></ore:Aggregation></rdf:RDF>