@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:Q3589154 rdfs:label "familial temporal lobe epilepsy 7"@en,
        "épilepsie partielle familiale autosomique dominante avec des signes auditifs"@fr ;
    schema1:dateModified "2026-07-05T11:10:14+00:00"^^xsd:dateTime ;
    schema1:description "مرض يصيب الإنسان"@ar,
        "Krankheit"@de,
        "temporal lobe epilepsy characterized by autosomal dominant inheritance of focal seizures with prominent auditory symptoms and that has material basis in heterozygous mutation in the RELN gene on chromosome 7q22"@en,
        "malattia"@it,
        "хвороба"@uk ;
    schema1:version 2514103361 ;
    wikibase:identifiers 6 ;
    wikibase:sitelinks 1 ;
    wikibase:statements 16 ;
    skos:altLabel "EPILEPSY, FAMILIAL TEMPORAL LOBE, 7"@en,
        "EPILEPSY, FAMILIAL TEMPORAL LOBE, 7; ETL7"@en,
        "ETL7"@en,
        "Epilepsy, Familial Temporal Lobe, type 7"@en,
        "familial temporal lobe epilepsy type 7"@en,
        "Epilepsie partielle familiale autosomique dominante avec des signes auditifs"@fr ;
    p:P11430 wds:Q3589154-3ce4bc87-4a95-8f27-d68e-0afd70d79ba9 ;
    p:P1550 wds:Q3589154-be1bb067-45c1-91c5-8142-8ff4aab41396 ;
    p:P2293 wds:Q3589154-0B5DFD84-CA21-493B-83A1-D75F33BCE366 ;
    p:P279 wds:Q3589154-42f06944-4e9e-9c9d-8d93-290832120238,
        wds:Q3589154-5C3D1523-B0B4-4927-8CC7-3218CEE2E37D,
        wds:Q3589154-60A31924-A21B-4852-8441-776AF2C15F83,
        wds:Q3589154-D66FCDAC-F2C5-4AF0-B955-E28258139FB8 ;
    p:P2888 wds:Q3589154-0A3CAC5B-1A62-41DB-98EF-4DFE541E5CE6,
        wds:Q3589154-0F32A34E-5620-4974-A481-EDADAD78DC6A,
        wds:Q3589154-1B27B98A-6A99-425C-9073-30310E416B5A ;
    p:P2892 wds:Q3589154-D016A2A4-9EE2-45B6-B5B3-A4C99925DE47 ;
    p:P31 wds:Q3589154-C611EA7A-68F1-4EF2-B6C1-5BA1077227FB ;
    p:P492 wds:Q3589154-B8C4A73C-0344-49FC-90CB-07E86FE21ED7 ;
    p:P5008 wds:Q3589154-536C1390-62F8-4361-B4C5-099EF8B14731 ;
    p:P5270 wds:Q3589154-59024B51-16AE-4BEA-BC37-F1FBDEB48C8A ;
    p:P699 wds:Q3589154-B69E12B2-1185-4C84-BE1E-A0AA01DFFF41 ;
    wdtn:P5270 <http://purl.obolibrary.org/obo/MONDO_0014639> ;
    wdtn:P699 <http://purl.obolibrary.org/obo/DOID_DOID:0060751> ;
    wdt:P11430 "DI-04463" ;
    wdt:P1550 "101046" ;
    wdt:P2293 wd:Q414043 ;
    wdt:P279 wd:Q18553439,
        wd:Q55787290,
        wd:Q616667 ;
    wdt:P2888 <http://identifiers.org/doid/DOID:0060751>,
        <http://purl.obolibrary.org/obo/DOID_0060751>,
        <http://www.orpha.net/ORDO/Orphanet_101046> ;
    wdt:P2892 "C4225327" ;
    wdt:P31 wd:Q112193867 ;
    wdt:P492 "616436" ;
    wdt:P5008 wd:Q4099686 ;
    wdt:P5270 "MONDO_0014639" ;
    wdt:P699 "DOID:0060751" .

