{
"@context": {
"dc": "http://purl.org/dc/elements/1.1/",
"dcterms": "http://purl.org/dc/terms/",
"iso-thes": "http://purl.org/iso25964/skos-thes#",
"nsogi": "http://prefix.cc/nsogi",
"rdf": "http://www.w3.org/1999/02/22-rdf-syntax-ns#",
"rdfs": "http://www.w3.org/2000/01/rdf-schema#",
"skos": "http://www.w3.org/2004/02/skos/core#",
"skosxl": "http://www.w3.org/2008/05/skos-xl#",
"xsd": "http://www.w3.org/2001/XMLSchema#"
},
"@id": "http://purl.org/bncf/tid/50571",
"@type": "skos:Concept",
"skos:prefLabel": {
"@language": "it","@value": "Malattia di Wilson"},
"dc:date": "2013-06-04",
"skos:inScheme": [
{
"@id": "http://purl.org/bncf/tid/Thes"},
{
"@id": "http://purl.org/bncf/tid/ThesCF8"
}
],
"skos:broader": {
"@id": "http://purl.org/bncf/tid/818"
},
"skos:altLabel": ["Degenerazione di Wilson", "Degenerazione epato-lenticolare", "Degenerazione epatolenticolare", "Degenerazione lenticolare progressiva", "Epatite familiare", "Epatite familiare giovanile progressiva con degenerazione del corpo striato", "Epatite familiare progressiva con degenerazione del corpo striato", "Epatite rarissima familiare", "Malattia di Kinnier-Wilson", "Malattia di Westphal-Strümpell", "Malattia epatolenticolare", "Morbo di Wilson", "Pseudosclerosi di Westphal-Strümpell", "Sindrome amniostatica", "Sindrome di Wilson", "Sindrome epatostriata", "Wilson, malattia di", "Wilson, morbo di"],
"skosxl:altLabel": [
{"@id": "http://purl.org/bncf/tid/71800"}, 
{"@id": "http://purl.org/bncf/tid/71797"}, 
{"@id": "http://purl.org/bncf/tid/50572"}, 
{"@id": "http://purl.org/bncf/tid/71689"}, 
{"@id": "http://purl.org/bncf/tid/50577"}, 
{"@id": "http://purl.org/bncf/tid/71804"}, 
{"@id": "http://purl.org/bncf/tid/71798"}, 
{"@id": "http://purl.org/bncf/tid/71801"}, 
{"@id": "http://purl.org/bncf/tid/71805"}, 
{"@id": "http://purl.org/bncf/tid/50578"}, 
{"@id": "http://purl.org/bncf/tid/50576"}, 
{"@id": "http://purl.org/bncf/tid/50575"}, 
{"@id": "http://purl.org/bncf/tid/50579"}, 
{"@id": "http://purl.org/bncf/tid/71802"}, 
{"@id": "http://purl.org/bncf/tid/71803"}, 
{"@id": "http://purl.org/bncf/tid/71799"}, 
{"@id": "http://purl.org/bncf/tid/50574"}, 
{"@id": "http://purl.org/bncf/tid/50573"}
],
"skos:related": [
{
"@id": "http://purl.org/bncf/tid/5047"
},
 {
"@id": "http://purl.org/bncf/tid/7725"
},
 {
"@id": "http://purl.org/bncf/tid/2735"
}],
"skos:closeMatch": [
{
"@id": "http://d-nb.info/gnd/4189925-8"}
],
"skos:closeMatch": [
{"@id": "http://id.loc.gov/authorities/sh85060301"},
{"@id": "http://data.bnf.fr/ark:/12148/cb124022187"},
{"@id": "http://www.wikidata.org/wiki/Q117121"}
],
"skos:scopeNote": "Malattia genetica che consiste in un difettoso metabolismo del rame, che si accumula in vari organi (cervello, fegato, occhi, ecc.) interferendo nel loro funzionamento",
"skos:editorialNote": "Soggettario; Treccani.it (voce: Epatolenticolare); Ascone-Lauricella; Benigno-Li Voti, DME (voce: Wilson, malattia di); DizMM; Dorland; EMedG (voce: Wilson, morbo di); MB; MESH(IT); Taber; Wikipedia(IT)"
}