@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:Q245455 rdfs:label "متلازمة حذف كروموسوم 5q"@ar,
        "Sindrom delecije 5q"@bs,
        "5q-minus-Syndrom"@de,
        "chromosome 5q deletion syndrome"@en,
        "Síndrome del 5q"@es,
        "syndrome 5q-"@fr,
        "5q-症候群"@ja,
        "5q-syndrom"@nn,
        "Síndrome mielodisplásica associada a anomalia cromossômica 5q isolada"@pt,
        "Síndrome mielodisplásica associada a anomalia cromossômica 5q isolada"@pt-br,
        "sindrom delecije kromosoma 5q"@sl,
        "sìndrome del 5q"@vec,
        "5號染色體長臂缺失症候群"@zh ;
    schema1:dateModified "2026-10-24T00:39:43+00:00"^^xsd:dateTime ;
    schema1:description "myelodysplastisches Syndrom"@de,
        "human disease"@en,
        "forme de myélodysplasie causée par une délétion du chromosome 5"@fr,
        "մարդու հիվանդություն"@hy,
        "malattia"@it,
        "хвороба людини"@uk ;
    schema1:version 2560167757 ;
    wikibase:identifiers 20,
        22 ;
    wikibase:sitelinks 8 ;
    wikibase:statements 55 ;
    skos:altLabel "5Q minus syndrome"@en,
        "5q- syndrome"@en,
        "5q- syndrome, refractory macrocytic anemia due to 5q deletion"@en,
        "CHROMOSOME 5q DELETION SYNDROME"@en,
        "Macrocytic Anemia, Refractory, Due to 5Q Deletion"@en,
        "Megakaryocytes, Unilobular Nucleated"@en,
        "Myelodysplastic Syndrome Associated with Isolated del (5q) Chromosome Abnormality"@en,
        "Myelodysplastic Syndrome with 5q Deletion"@en,
        "Myelodysplastic Syndrome with Isolated del(5q)"@en,
        "myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality"@en,
        "del(5q)"@nn,
        "delesjon 5q"@nn ;
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    p:P7807 wds:Q245455-69C4545E-24C6-46E2-9FC7-FE0F0A9CD282 ;
    wdtn:P486 <http://id.nlm.nih.gov/mesh/C535323> ;
    wdtn:P5270 <http://purl.obolibrary.org/obo/MONDO_0007925> ;
    wdtn:P6366 <https://makg.org/entity/2779004087> ;
    wdtn:P665 <http://www.kegg.jp/entry/H01484> ;
    wdtn:P699 <http://purl.obolibrary.org/obo/DOID_DOID:0090016> ;
    wdt:P11143 "Chromosome 5q deletion syndrome" ;
    wdt:P1193 0.000001 ;
    wdt:P14914 "D86841" ;
    wdt:P1550 "86841" ;
    wdt:P1748 "C6867" ;
    wdt:P1995 wd:Q103824 ;
    wdt:P2176 wd:Q425681 ;
    wdt:P2293 wd:Q18031301 ;
    wdt:P279 wd:Q1348398,
        wd:Q16918398,
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        wd:Q55785845,
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        wd:Q56013913,
        wd:Q954625 ;
    wdt:P2841 wd:Q21955204 ;
    wdt:P2888 <http://identifiers.org/doid/DOID:0090016>,
        <http://purl.obolibrary.org/obo/DOID_0090016>,
        <http://www.orpha.net/ORDO/Orphanet_86841> ;
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        "C1292779",
        "C1835193" ;
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    wdt:P373 "Chromosome 5q deletion syndrome" ;
    wdt:P4229 "D46.7" ;
    wdt:P4317 "10840",
        "8723" ;
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    wdt:P492 "153550" ;
    wdt:P5008 wd:Q4099686 ;
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    wdt:P699 "DOID:0090016" ;
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    wdt:P7464 "5q-minus-syndrome" ;
    wdt:P7807 "420472577" .

