@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:Q751631 rdfs:label "عدم تنسج الكرية الحمراء النقي"@ar,
        "Eritroblastopenija"@bs,
        "aplasia celloedd coch pur"@cy,
        "Erworbene isolierte aplastische Anämie"@de,
        "pure red-cell aplasia"@en,
        "Puhas punalibleaplaasia"@et,
        "اریتروبلاستوپنی"@fa,
        "érythroblastopénie chronique acquise"@fr,
        "aplasia eritroide pura"@it,
        "赤芽球癆"@ja,
        "Izoliuota aplastinė anemija"@lt,
        "Aplasia pura primária adquirida dos glóbulos vermelhos"@pt,
        "Aplasia pura primária adquirida dos glóbulos vermelhos"@pt-br,
        "Kazanılmış saf kırmızı hücre aplazisi"@tr,
        "純紅細胞再生障礙性貧血"@zh ;
    schema1:dateModified "2026-10-24T00:51:43+00:00"^^xsd:dateTime ;
    schema1:description "مرض يصيب الإنسان"@ar,
        "Krankheit"@de,
        "human disease"@en,
        "մարդու հիվանդություն"@hy,
        "хвороба людини"@uk ;
    schema1:version 2560169536 ;
    wikibase:identifiers 23,
        26 ;
    wikibase:sitelinks 10 ;
    wikibase:statements 38 ;
    skos:altLabel "عدم تنسج الكرية الحمراء الخالص"@ar,
        "عدم تنسج الكرية الحمراء الصرف"@ar,
        "قلة الأرومات الحمر"@ar,
        "نقص الأرومات الحمر"@ar,
        "Erythroblastopenie"@de,
        "PRCA"@de,
        "Pure Red Cell Aplasia"@de,
        "PRCA"@en,
        "Pure Red cell Aplasia"@en,
        "Pure red cell aplasia (disorder)"@en,
        "Pure red cell aplasia; PRCA"@en,
        "Red cell hypoplasia"@en,
        "Red-Cell Aplasia, Pure"@en,
        "primary red cell aplasia"@en,
        "PRCA"@et,
        "aplasie érythrocytaire"@fr,
        "Anemia di Blackfan Diamond"@it,
        "Anemia di Blackfan-Diamond"@it,
        "Anemia di Diamond - Blackfan"@it,
        "Aplasia delle cellule della serie rossa"@it,
        "Aplasia pura della serie bianca"@it,
        "Eritroblastopenia acuta acquisita"@it,
        "Eritroblastopenia congenita"@it,
        "Eritroblastopenia cronica acquisita"@it,
        "純紅細胞發育不全（PRCA）"@zh ;
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    p:P5008 wds:Q751631-72E93D60-1B65-49BD-BE21-13EFE0569E90 ;
    p:P5270 wds:Q751631-D725549C-A9EA-4479-A67F-1E233E8B0B62 ;
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    p:P7807 wds:Q751631-66FC5EDA-2E84-4489-B91E-5061823F4CAC ;
    wdtn:P3201 <http://purl.bioontology.org/ontology/MDRFRE/10002965> ;
    wdtn:P486 <http://id.nlm.nih.gov/mesh/D012010> ;
    wdtn:P5270 <http://purl.obolibrary.org/obo/MONDO_0001705> ;
    wdtn:P6366 <https://makg.org/entity/2777422296> ;
    wdtn:P665 <http://www.kegg.jp/entry/H01586> ;
    wdtn:P672 <http://id.nlm.nih.gov/mesh/C15.378.050.750> ;
    wdtn:P699 <http://purl.obolibrary.org/obo/DOID_DOID:1340> ;
    wdt:P10283 "C2777422296" ;
    wdt:P10565 "558544" ;
    wdt:P11143 "Pure red cell aplasia" ;
    wdt:P1325 <http://www.nanbyou.or.jp/entry/4450> ;
    wdt:P14541 "1Ws8Fg" ;
    wdt:P14914 "D98872" ;
    wdt:P1550 "98872" ;
    wdt:P1692 "284.81" ;
    wdt:P1748 "C34974" ;
    wdt:P1995 wd:Q103824 ;
    wdt:P2176 wd:Q408524 ;
    wdt:P279 wd:Q3591490 ;
    wdt:P2888 <http://identifiers.org/doid/DOID:1340>,
        <http://purl.obolibrary.org/obo/DOID_1340>,
        <http://purl.obolibrary.org/obo/HP_0012410> ;
    wdt:P2892 "C0034902",
        "C4707560" ;
    wdt:P31 wd:Q112193867,
        wd:Q42303753 ;
    wdt:P3201 "10002965" ;
    wdt:P3827 "pure-red-cell-aplasia" ;
    wdt:P3841 "HP:0012410" ;
    wdt:P4317 "10898",
        "7504" ;
    wdt:P486 "D012010" ;
    wdt:P493 "284.8" ;
    wdt:P494 "D60" ;
    wdt:P5008 wd:Q4099686 ;
    wdt:P5270 "MONDO_0001705" ;
    wdt:P557 "29063" ;
    wdt:P6366 "2777422296" ;
    wdt:P646 "/m/08wzrl" ;
    wdt:P665 "H01586" ;
    wdt:P672 "C15.378.050.750" ;
    wdt:P673 "205695" ;
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    wdt:P7807 "1980066564" .