This HTML5 document contains 87 embedded RDF statements represented using HTML+Microdata notation.

The embedded RDF content will be recognized by any processor of HTML5 Microdata.

Namespace Prefixes

PrefixIRI
wdthttp://www.wikidata.org/prop/direct/
wdtnhttp://www.wikidata.org/prop/direct-normalized/
n10http://purl.obolibrary.org/obo/
schemahttp://schema.org/
rdfshttp://www.w3.org/2000/01/rdf-schema#
skoshttp://www.w3.org/2004/02/skos/core#
wikibasehttp://wikiba.se/ontology#
phttp://www.wikidata.org/prop/
n12http://www.kegg.jp/entry/
rdfhttp://www.w3.org/1999/02/22-rdf-syntax-ns#
n16https://makg.org/entity/
owlhttp://www.w3.org/2002/07/owl#
n11http://purl.obolibrary.org/obo/DOID_DOID:
n18http://identifiers.org/doid/DOID:
n17http://www.orpha.net/ORDO/
n19http://id.nlm.nih.gov/mesh/
xsdhhttp://www.w3.org/2001/XMLSchema#
wdshttp://www.wikidata.org/entity/statement/
dbpediahttp://dbpedia.org/resource/
wdhttp://www.wikidata.org/entity/

Statements

Subject Item
wd:Q6458655
rdf:type
wikibase:Item
owl:sameAs
dbpedia:LIG4_syndrome
schema:description
մարդու հիվանդություն Human disease rzadki zespół wad wrodzonych spowodowany mutacjami w genie LIG4 Krankheit مرض يصيب الإنسان maladie хвороба людини
p:P2888
wds:Q6458655-F36C05CD-99B5-4459-8395-C15F8E02088E wds:Q6458655-FD158441-E194-4CB3-8544-A5B412E46207 wds:Q6458655-F08E798A-5501-481E-AD0B-165497BAD364
wdt:P2888
n17:Orphanet_99812 n10:DOID_0060021 n18:0060021
p:P5270
wds:Q6458655-3D75772A-29BB-40F0-B86E-8B6BC29E93D8
p:P699
wds:Q6458655-D9749279-84E5-4D65-9051-6D96074ADF52
wdtn:P5270
n10:MONDO_0011686
wdtn:P699
n11:0060021
wdt:P5270
MONDO_0011686
wdt:P699
DOID:0060021
rdfs:label
syndrome LIG4 LIG4-oireyhtymä DNA ligase IV deficiency Zespół LIG4
skos:prefLabel
Zespół LIG4 DNA ligase IV deficiency LIG4-oireyhtymä syndrome LIG4
schema:name
syndrome LIG4 LIG4-oireyhtymä Zespół LIG4 DNA ligase IV deficiency
p:P31
wds:Q6458655-65E5D0F6-ACD7-4D12-B254-35DBC1AC3C7A wds:Q6458655-D4D4EAB6-D3C7-4462-AB6B-A9191B785A75 wds:Q6458655-E181A935-2FFD-4E50-8D76-8217D2C3AE88
wdt:P31
wd:Q929833 wd:Q200779 wd:Q112193867
p:P279
wds:Q6458655-3DF362D1-F04C-4985-A3F9-C733AB881656 wds:Q6458655-41CC1938-92DE-4ABA-8CC8-989BAC38E451 wds:Q6458655-062A4475-FEA7-437C-8E5F-E23774DE620B wds:Q6458655-2E657ABD-B802-4981-8454-D8F517BE002A wds:Q6458655-D908BA7C-7B60-4A07-A48B-539BDA010609 wds:Q6458655-DC7725CB-E9ED-465F-9D7C-290A275414A6 wds:Q6458655-7F5A2D4F-D961-44FF-9C06-06371792F307
wdt:P279
wd:Q55788363 wd:Q5150906 wd:Q1117773 wd:Q10267817 wd:Q55785846 wd:Q200779 wd:Q55785832
p:P665
wds:Q6458655-5AA025E0-0CBD-49EE-89C4-9422E3AD0B42
wdtn:P665
n12:H02015
wdt:P665
H02015
p:P11430
wds:Q6458655-9d40f563-4acc-802c-7810-0f44b537fdff
p:P1550
wds:Q6458655-b1aed97b-4bb0-8d14-f2a1-9727185740a0
p:P2293
wds:Q6458655-C662CC0F-7906-4613-AF31-8E16B378DF32
p:P4229
wds:Q6458655-6B53D8A8-22CE-4B2C-8A04-A8D9A571FB71
p:P492
wds:Q6458655-3945358D-72CB-4437-80C5-0F156CBF216F
wdt:P11430
DI-01906
wdt:P1550
99812
wdt:P2293
wd:Q18028560
wdt:P4229
D81.1
wdt:P492
606593
p:P373
wds:Q6458655-69356f11-aaf2-4f98-824e-b6f900c09d04
wdt:P373
LIG4 syndrome
skos:altLabel
Ligase 4 syndrome Déficit en DNA ligase IV LIG4 Syndrome
p:P1748
wds:Q6458655-298f7a05-4d03-7ea0-eb69-f3df674acf3f
p:P2892
wds:Q6458655-ECD2E088-F022-45DD-82D8-9C4AA972DC02
p:P486
wds:Q6458655-941D909E-F877-4F66-98A0-2621A0A56D3C
p:P5008
wds:Q6458655-FD52E7EF-57D9-4AFB-BFF3-DC61DF84175B
p:P6366
wds:Q6458655-C8DBE3C9-5117-44F0-A05B-3A7D682943EE
wdtn:P486
n19:C564694
wdtn:P6366
n16:2781061984
wdt:P1748
C122657
wdt:P2892
C1847827
wdt:P486
C564694
wdt:P5008
wd:Q4099686
wdt:P6366
2781061984
p:P11143
wds:Q6458655-67958B79-2787-4458-BA23-6DFB1495760F
wdt:P11143
LIG4 syndrome
p:P6532
wds:Q6458655-348D25E6-80C7-42E6-ADD7-440DB45840BB
wdt:P6532
wd:Q3043160