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Namespace Prefixes

PrefixIRI
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wdtnhttp://www.wikidata.org/prop/direct-normalized/
n7http://purl.obolibrary.org/obo/
schemahttp://schema.org/
skoshttp://www.w3.org/2004/02/skos/core#
rdfshttp://www.w3.org/2000/01/rdf-schema#
wikibasehttp://wikiba.se/ontology#
phttp://www.wikidata.org/prop/
rdfhttp://www.w3.org/1999/02/22-rdf-syntax-ns#
n11http://purl.obolibrary.org/obo/DOID_DOID:
n14http://identifiers.org/doid/DOID:
n12http://id.nlm.nih.gov/mesh/
xsdhhttp://www.w3.org/2001/XMLSchema#
wdshttp://www.wikidata.org/entity/statement/
wdhttp://www.wikidata.org/entity/

Statements

Subject Item
wd:Q27674741
rdf:type
wikibase:Item
schema:description
مرض يصيب الإنسان syndrome characterized by the clinical features of 46,XY complete gonadal dysgenesis in association with severe dwarfism with generalized chondrodysplasia хвороба Krankheit
p:P2888
wds:Q27674741-8C183DB1-F9F0-44BF-9FB7-A4080949657D wds:Q27674741-8D8F817C-CA77-4558-B8E0-525F67B86D3E
wdt:P2888
n7:DOID_0060644 n14:0060644
p:P1995
wds:Q27674741-3523C39F-ECCF-4C4B-AC15-0487B8F4B7DE
p:P5270
wds:Q27674741-210B6DD0-9F76-4EB3-9B72-5B301D2AE4C4
p:P699
wds:Q27674741-79D9809D-0299-4945-A397-EEC533253A04
wdtn:P5270
n7:MONDO_0010814
wdtn:P699
n11:0060644
wdt:P1995
wd:Q1071953
wdt:P5270
MONDO_0010814
wdt:P699
DOID:0060644
rdfs:label
chondrodysplasia-pseudohermaphroditism syndrome syndrome de chondrodysplasie-anomalie du développement sexuel
skos:prefLabel
chondrodysplasia-pseudohermaphroditism syndrome syndrome de chondrodysplasie-anomalie du développement sexuel
schema:name
syndrome de chondrodysplasie-anomalie du développement sexuel chondrodysplasia-pseudohermaphroditism syndrome
p:P31
wds:Q27674741-39DA8D7C-C4DF-4F20-85D8-BCE6491E5D88 wds:Q27674741-61638F88-A7AB-413D-A4D6-5A4431B84B41
wdt:P31
wd:Q112193867 wd:Q55788864
p:P279
wds:Q27674741-04562AE1-6AE2-48E6-A2DC-4E4A5C06766D wds:Q27674741-118cb41d-471b-0e58-d4a3-f1606b6c05ce wds:Q27674741-6ed4eaee-4c44-569e-497e-b62d13421cea wds:Q27674741-46ED0BFD-1EE4-4F33-BEA9-8D7BF8B19576 wds:Q27674741-A6562C9A-B77C-487E-900B-CD9FF90C12B7 wds:Q27674741-AD0390D4-FE8F-43FC-8AD1-4DC9B65B68EE
wdt:P279
wd:Q55789077 wd:Q55787661 wd:Q55787807 wd:Q179630 wd:Q26271752 wd:Q2273662
p:P11430
wds:Q27674741-38c316ab-4601-743f-21a6-7b2658ae564f
p:P1550
wds:Q27674741-2937EECD-0B6C-4084-8735-A3E68AEDAA0A
p:P4229
wds:Q27674741-004BCDFF-F866-410D-8130-20F6048C83BD
p:P492
wds:Q27674741-D9A33277-9E66-49D5-91BB-B26204610C3E
wdt:P11430
DI-05999
wdt:P1550
1422
wdt:P4229
Q87.1
wdt:P492
600092
skos:altLabel
Chondrodysplasia-pseudohermaphroditism syndrome chondrodysplasia-disorder of sex development syndrome Nivelon-Nivelon-Mabille syndrome
p:P2892
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p:P486
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p:P5008
wds:Q27674741-F2142397-97B9-4B6B-9B4D-8CC7FF9DD3B7
wdtn:P486
n12:C536123
wdt:P2892
C1838654
wdt:P486
C536123
wdt:P5008
wd:Q4099686