prefix :
prefix fresnel:
prefix rdf:
prefix owl:
prefix marc:
prefix xsd:
prefix rdfs:
prefix jsonld:
prefix kbv:
prefix sdo:
a :Record ;
:sameAs ;
:created "2002-04-09T11:30:54+02:00"^^xsd:dateTime ;
:modified "2020-02-04T11:16:37.348+01:00"^^xsd:dateTime ;
:mainEntity ;
:identifiedBy [ a :SystemNumber ;
:value "(sao)13625" ] ;
:recordStatus marc:CorrectedOrRevised ;
:controlNumber "146678" ;
:generationDate "2021-03-10T18:59:16.029+01:00" ;
:generationProcess ;
:descriptionCreator ;
:descriptionLanguage ;
:descriptionLastModifier .
a :Topic ;
:sameAs ;
:related ;
:inScheme ;
:prefLabel "Genetiska sjukdomar" ;
:broadMatch [ :code "Vaa" ;
a :Classification ;
:inScheme [ :code "kssb" ;
a :ConceptScheme ;
:sameAs ;
:version "7" ] ] ;
:closeMatch [ a :Topic ;
:inScheme ;
:prefLabel "Genetic disorders" ] ;
:hasVariant [ a :Topic ;
:prefLabel "Ärftliga sjukdomar" ] ;
:inCollection .
:broader .
:broader .
:broader .
:broader .
:broader .
:broader .
:broader .
:broader .
:broader .
:broader .
a :Record ;
:created "2021-06-16T18:41:46.123+02:00"^^xsd:dateTime ;
:modified "2021-06-16T18:41:46.123+02:00"^^xsd:dateTime ;
:inDataset ,
;
:mainEntity ;
:recordStatus marc:CorrectedOrRevised .
:name "Nationalbibliografin" ;
a :Bibliography ;
:sigel "NB" ;
:sameAs .
a :Record ;
:created "2021-06-16T18:40:31.536+02:00"^^xsd:dateTime ;
:modified "2021-06-16T18:40:31.536+02:00"^^xsd:dateTime ;
:inDataset ,
;
:mainEntity ;
:recordStatus marc:CorrectedOrRevised .
:name "Kungliga biblioteket" ;
a :Library ;
:sigel "S" ;
:sameAs .
a :Record ;
:created "2022-12-07T16:26:42.1+01:00"^^xsd:dateTime ;
:modified "2022-12-07T16:26:42.1+01:00"^^xsd:dateTime ;
:inDataset ,
;
:mainEntity ;
:recordStatus marc:New .
:code "swe" ;
a :Language ;
:sameAs ;
:code "sv"^^:BCP47 ;
:prefLabel "Schwedisch"@de , "Swedish"@en , "suédois"@fr , "Svenska"@sv .
a :Record ;
:sameAs ;
:created "2002-04-09T11:41:00+02:00"^^xsd:dateTime ;
:modified "2014-05-12T11:50:51+02:00"^^xsd:dateTime ;
:mainEntity ;
:identifiedBy [ a :SystemNumber ;
:value "(sao)33607" ] ;
:recordStatus marc:CorrectedOrRevised ;
:controlNumber "153784" ;
:generationDate "2021-03-10T19:05:25.904+01:00" ;
:generationProcess ;
:descriptionCreator .
a :Topic ;
:sameAs ;
:broader ,
,
;
:related ;
:inScheme ;
:prefLabel "Medicinsk genetik" ;
:broadMatch [ :code "Vaa" ;
a :Classification ;
:inScheme [ :code "kssb" ;
a :ConceptScheme ;
:sameAs ] ] ;
:closeMatch [ a :Topic ;
:inScheme ;
:prefLabel "Medical genetics" ] ;
:hasVariant [ a :ComplexSubject ;
:prefLabel "Genetik--medicin" ;
:termComponentList ( ( [ a :Topic ;
:prefLabel "Genetik" ] ) ( [ a :TopicSubdivision ;
:prefLabel "medicin" ] ) ) ] ,
[ a :ComplexSubject ;
:prefLabel "Sjukdomar--genetik" ;
:termComponentList ( ( [ a :Topic ;
:prefLabel "Sjukdomar" ] ) ( [ a :TopicSubdivision ;
:prefLabel "genetik" ] ) ) ] ;
:inCollection .
:broader .
a :Record ;
:created "2022-12-07T16:26:51.968+01:00"^^xsd:dateTime ;
:modified "2022-12-07T16:26:51.968+01:00"^^xsd:dateTime ;
:inDataset ,
;
:mainEntity ;
:recordStatus marc:New .
:code "lcsh" ;
a :TopicScheme ;
:title "Library of Congress Subject Headings" ;
:exactMatch ,
,
;
:title "Library of Congress Subject Headings"@en .
a :Record ;
:created "2022-12-07T16:26:51.509+01:00"^^xsd:dateTime ;
:modified "2022-12-07T16:26:51.509+01:00"^^xsd:dateTime ;
:inDataset ,
;
:mainEntity ;
:recordStatus marc:New .
:code "Fack" ;
a :TermCollection ;
:sameAs ;
:title "Facktermer"@sv .
a :Record ;
:created "2022-12-07T16:26:52.482+01:00"^^xsd:dateTime ;
:modified "2022-12-07T16:26:52.482+01:00"^^xsd:dateTime ;
:inDataset ,
;
:mainEntity ;
:recordStatus marc:CorrectedOrRevised .
:code "sao" ;
a :TopicScheme ;
:exactMatch ,
;
:title "Svenska ämnesord"@sv .
a :Record ;
:sameAs ;
:created "2005-10-25T18:22:31+02:00"^^xsd:dateTime ;
:modified "2014-05-12T12:51:38+02:00"^^xsd:dateTime ;
:mainEntity ;
:recordStatus marc:CorrectedOrRevised ;
:controlNumber "263572" ;
:generationDate "2021-03-10T20:52:22.518+01:00" ;
:sourceConsulted [ a :SourceData ;
:label "NE." ] ,
[ a :SourceData ;
:label "Svensk MeSH." ] ;
:generationProcess ;
:descriptionCreator .
a :Topic ;
:sameAs ;
:broader ,
;
:inScheme ;
:prefLabel "Epidermolysis bullosa" ;
:broadMatch [ :code "Vem" ;
a :Classification ;
:inScheme [ :code "kssb" ;
a :ConceptScheme ;
:sameAs ] ] ;
:closeMatch [ a :Topic ;
:inScheme ;
:prefLabel "Epidermolysis bullosa" ] ;
:hasVariant [ a :Topic ;
:prefLabel "EB" ] ;
:inCollection .
a :Record ;
:sameAs ;
:created "2015-09-08T14:15:23+02:00"^^xsd:dateTime ;
:modified "2015-09-08T14:15:23+02:00"^^xsd:dateTime ;
:mainEntity ;
:recordStatus marc:New ;
:controlNumber "388253" ;
:generationDate "2021-03-10T20:52:24.44+01:00" ;
:sourceConsulted [ a :SourceData ;
:label "NE 2015-06-24." ] ;
:generationProcess ;
:descriptionCreator .
a :Topic ;
:sameAs ;
:broader ;
:inScheme ;
:prefLabel "Progeri" ;
:closeMatch [ :code "616.042" ;
a :ClassificationDdc ;
:edition "23/swe" ;
marc:explanatoryTerm "BroadMatch" ] ,
[ a :Topic ;
:inScheme ;
:prefLabel "Progeria" ] ;
:hasVariant [ a :Topic ;
:prefLabel "Hutchinson–Gilfords syndrom" ] ,
[ a :Topic ;
:prefLabel "Progeria" ] ;
:inCollection .
a :Record ;
:sameAs ;
:created "2006-02-16T17:37:24+01:00"^^xsd:dateTime ;
:modified "2014-05-12T12:52:43+02:00"^^xsd:dateTime ;
:mainEntity ;
:recordStatus marc:CorrectedOrRevised ;
:controlNumber "268618" ;
:generationDate "2021-10-11T10:45:00.738+02:00" ;
:sourceConsulted [ a :SourceData ;
:label "NE." ] ;
:generationProcess ;
:descriptionCreator .
a :Topic ;
:sameAs ;
:broader ,
;
:inScheme ;
:prefLabel "Leukodystrofi" ;
:scopeNote "- nervsystemet Vef, - medicinsk genetik Vaa." ;
:broadMatch [ :code "Vef" ;
a :Classification ;
:inScheme [ :code "kssb" ;
a :ConceptScheme ;
:sameAs ] ] ,
[ :code "Vaa" ;
a :Classification ;
:inScheme [ :code "kssb" ;
a :ConceptScheme ;
:sameAs ] ] ;
:closeMatch [ a :Topic ;
:inScheme ;
:prefLabel "Leukodystrophy, Globoid cell" ] ,
[ a :Topic ;
:inScheme ;
:prefLabel "Leukodystrophy, Metachromatic" ] ;
:hasVariant [ a :Topic ;
:prefLabel "Canavans sjukdom" ] ,
[ a :Topic ;
:prefLabel "Globoidcell leukodystrofi" ] ,
[ a :Topic ;
:prefLabel "Globoidcellsleukodystrofi" ] ,
[ a :Topic ;
:prefLabel "Metakromatisk leukodystrofi" ] ;
:inCollection .
a :Record ;
:sameAs ;
:created "2012-02-17T13:20:09+01:00"^^xsd:dateTime ;
:modified "2016-01-13T09:20:47+01:00"^^xsd:dateTime ;
:mainEntity ;
:recordStatus marc:CorrectedOrRevised ;
:controlNumber "350788" ;
:generationDate "2021-03-10T20:52:24.876+01:00" ;
:sourceConsulted [ a :SourceData ;
:label "SvMeSH 2012-01-31." ] ,
[ a :SourceData ;
:label "http://ssvf.nu/om-spielmeyer-vogt/" ] ;
:generationProcess ;
:descriptionCreator .
a :Topic ;
:sameAs ;
:broader ,
,
,
;
:inScheme ;
:prefLabel "Neuronala ceroida lipofuskinoser" ;
:closeMatch [ :code "616.83" ;
a :ClassificationDdc ;
:edition "22/swe" ] ,
[ a :Topic ;
:inScheme ;
:prefLabel "Neuronal ceroid-lipofuscinosis" ] ;
:hasVariant [ a :Topic ;
:prefLabel "Battens sjukdom" ] ,
[ a :Topic ;
:prefLabel "CLN3" ] ,
[ a :Topic ;
:prefLabel "JNCL" ] ,
[ a :Topic ;
:prefLabel "Juvenil Battens sjukdom" ] ,
[ a :Topic ;
:prefLabel "Juvenil neuronal ceroid-lipofuscinos" ] ,
[ a :Topic ;
:prefLabel "Juvenil neuronal ceroidlipofuscinos" ] ,
[ a :Topic ;
:prefLabel "NCL" ] ,
[ a :Topic ;
:prefLabel "Spielmeyer-Vogts sjukdom" ] ,
[ a :Topic ;
:prefLabel "Stengel-Batten-Spielmeyer-Vogts sjukdom" ] ;
:inCollection .
a :Record ;
:sameAs ;
:created "2005-10-25T10:45:19+02:00"^^xsd:dateTime ;
:modified "2014-05-12T12:51:33+02:00"^^xsd:dateTime ;
:mainEntity ;
:recordStatus marc:CorrectedOrRevised ;
:controlNumber "263463" ;
:generationDate "2020-02-25T19:51:15.189+01:00" ;
:sourceConsulted [ a :SourceData ;
:label "Socialstyrelsen - Små och mindre kända handikappgrupper." ] ;
:generationProcess ;
:descriptionCreator .
a :Topic ;
:sameAs ;
:broader ,
;
:inScheme ;
:prefLabel "Aicardis syndrom" ;
:broadMatch [ :code "Vebv" ;
a :Classification ;
:inScheme [ :code "kssb" ;
a :ConceptScheme ;
:sameAs ] ] ;
:inCollection .
a :Record ;
:created "2020-02-04T11:16:21.022+01:00"^^xsd:dateTime ;
:modified "2020-02-04T11:18:40.228+01:00"^^xsd:dateTime ;
:mainEntity ;
:recordStatus marc:CorrectedOrRevised ;
:controlNumber "p1w2kl9mmg38kx9j" ;
:generationDate "2021-04-19T11:49:16.655+02:00" ;
:sourceConsulted [ a :SourceData ;
:label "Kallmanns syndrom" ;
:citationNote "Svensk MeSH 2020-01-17 i artikel Kallmanns syndrom" ] ;
:generationProcess ;
:descriptionCreator ;
:descriptionLastModifier .
a :Topic ;
:sameAs ;
:broader ;
:inScheme ;
:prefLabel "Kallmanns syndrom" ;
:broadMatch [ :code "616.47" ;
a :ClassificationDdc ] ;
:inCollection .
a :Record ;
:sameAs ;
:created "2005-10-25T11:53:49+02:00"^^xsd:dateTime ;
:modified "2014-05-12T12:51:33+02:00"^^xsd:dateTime ;
:mainEntity ;
:recordStatus marc:CorrectedOrRevised ;
:controlNumber "263471" ;
:generationDate "2021-03-10T20:53:04.452+01:00" ;
:sourceConsulted [ a :SourceData ;
:label "NE." ] ;
:generationProcess ;
:descriptionCreator .
a :Topic ;
:sameAs ;
:broader ,
;
:related ;
:inScheme ;
:prefLabel "Akondroplasi" ;
:broadMatch [ :code "Ven" ;
a :Classification ;
:inScheme [ :code "kssb" ;
a :ConceptScheme ;
:sameAs ] ] ;
:closeMatch [ a :Topic ;
:inScheme ;
:prefLabel "Achondroplasia" ] ;
:inCollection .
a :Record ;
:sameAs ;
:created "2005-10-25T16:15:48+02:00"^^xsd:dateTime ;
:modified "2014-05-12T12:51:35+02:00"^^xsd:dateTime ;
:mainEntity ;
:recordStatus marc:CorrectedOrRevised ;
:controlNumber "263533" ;
:generationDate "2021-03-10T20:53:04.55+01:00" ;
:sourceConsulted [ a :SourceData ;
:label "NE." ] ;
:generationProcess ;
:descriptionCreator .
a :Topic ;
:sameAs ;
:broader ,
,
;
:inScheme ;
:prefLabel "Klinefelters syndrom" ;
:broadMatch [ :code "Vaa" ;
a :Classification ;
:inScheme [ :code "kssb" ;
a :ConceptScheme ;
:sameAs ] ] ;
:closeMatch [ a :Topic ;
:inScheme ;
:prefLabel "Klinefelter's syndrome" ] ;
:inCollection .
a :Record ;
:sameAs ;
:created "2002-04-09T11:37:33+02:00"^^xsd:dateTime ;
:modified "2015-07-07T14:12:00+02:00"^^xsd:dateTime ;
:mainEntity ;
:identifiedBy [ a :SystemNumber ;
:value "(sao)19828" ] ;
:recordStatus marc:CorrectedOrRevised ;
:controlNumber "151365" ;
:generationDate "2021-10-11T11:57:16.071+02:00" ;
:generationProcess ;
:descriptionCreator .
a :Topic ;
:sameAs ;
:broader ,
;
:inScheme ;
:prefLabel "Kromosomrubbningar" ;
:scopeNote "- medicinsk genetik Vaa, - teratologi (missbildningslära) Vbbc." ;
:broadMatch [ :code "Vaa" ;
a :Classification ;
:inScheme [ :code "kssb" ;
a :ConceptScheme ;
:sameAs ] ] ,
[ :code "Vbbc" ;
a :Classification ;
:inScheme [ :code "kssb" ;
a :ConceptScheme ;
:sameAs ] ] ;
:closeMatch [ a :Topic ;
:inScheme ;
:prefLabel "Chromosome abnormalities" ] ;
:hasVariant [ a :Topic ;
:prefLabel "Kromosomavvikelser" ] ,
[ a :Topic ;
:prefLabel "Kromosommutationer" ] ,
[ a :Topic ;
:prefLabel "Kromosal abberation" ] ;
:inCollection .
:broader .
:broader .
:broader .
:broader .
:broader .
:broader .
:broader .
:broader .
:broader .
:broader .
:broader .
:broader .
a :Record ;
:sameAs ;
:created "2005-10-25T18:07:21+02:00"^^xsd:dateTime ;
:modified "2014-05-12T12:51:37+02:00"^^xsd:dateTime ;
:mainEntity ;
:recordStatus marc:CorrectedOrRevised ;
:controlNumber "263565" ;
:generationDate "2021-03-10T20:53:08.111+01:00" ;
:sourceConsulted [ a :SourceData ;
:label "NE." ] ,
[ a :SourceData ;
:label "Svensk MeSH." ] ;
:generationProcess ;
:descriptionCreator .
a :Topic ;
:sameAs ;
:broader ,
;
:inScheme ;
:prefLabel "Ehlers-Danlos syndrom" ;
:broadMatch [ :code "Ven" ;
a :Classification ;
:inScheme [ :code "kssb" ;
a :ConceptScheme ;
:sameAs ] ] ;
:closeMatch [ a :Topic ;
:inScheme ;
:prefLabel "Ehlers-Danlos syndrome" ] ;
:hasVariant [ a :Topic ;
:prefLabel "EDS" ] ;
:inCollection .
a :Record ;
:sameAs ;
:mainEntity ;
:controlNumber "263566" .
a :Topic ;
:sameAs ;
:prefLabel "Bindvävssjukdomar" ;
:inScheme .
a :Record ;
:sameAs ;
:mainEntity ;
:controlNumber "148134" .
a :Topic ;
:sameAs ;
:prefLabel "Hudsjukdomar" ;
:inScheme .
a :Record ;
:sameAs ;
:mainEntity ;
:controlNumber "165264" .