@prefix p: <http://www.wikidata.org/prop/> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix schema1: <http://schema.org/> .
@prefix skos: <http://www.w3.org/2004/02/skos/core#> .
@prefix wd: <http://www.wikidata.org/entity/> .
@prefix wds: <http://www.wikidata.org/entity/statement/> .
@prefix wdt: <http://www.wikidata.org/prop/direct/> .
@prefix wdtn: <http://www.wikidata.org/prop/direct-normalized/> .
@prefix wikibase: <http://wikiba.se/ontology#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .

wd:Q56137331 rdfs:label "متلازمة تثلث الصيغة الصبغية"@ar,
        "Triploid sindromu"@az,
        "ট্রিপলয়েড সিনড্রোম"@bn,
        "Triploid-Mongoloidie"@de,
        "triploid syndrome"@en,
        "Síndrome triploide"@es,
        "syndrome triploïde"@fr,
        "טריפלואידיות"@he,
        "Triploidia"@pt,
        "Triploidia"@pt-br,
        "triploidni sindrom"@sl,
        "sìndrome triplòide"@vec,
        "三倍體"@zh ;
    schema1:dateModified "2026-10-24T00:09:25+00:00"^^xsd:dateTime ;
    schema1:description "seltene Chromosomenaberration, meist mit einem Karyotyp von 69,XXX oder 69,XXY"@de,
        "extremely rare chromosomal disorder occuring during human embryogenesis, causing severe abnormalities in fetal development and usually lethal in the prenatal stage"@en,
        "désordre chromosomique extrêmement rare survenant durant l'embryogénèse humaine, causant de sévère anomalies du développement fœtal et généralement létale au stade prénatal"@fr ;
    schema1:version 2560162983 ;
    wikibase:identifiers 13,
        15 ;
    wikibase:sitelinks 6 ;
    wikibase:statements 49 ;
    skos:altLabel "chromosome triploidy syndrome"@en,
        "triploidy"@en,
        "triploidy syndrome"@en,
        "syndrome chromosomique de triploïdie"@fr,
        "syndrome de triploïdie"@fr ;
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