This HTML5 document contains 51 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/
n4http://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/
rdfhttp://www.w3.org/1999/02/22-rdf-syntax-ns#
n10http://purl.obolibrary.org/obo/DOID_DOID:
n12http://identifiers.org/doid/DOID:
xsdhhttp://www.w3.org/2001/XMLSchema#
wdshttp://www.wikidata.org/entity/statement/
wdhttp://www.wikidata.org/entity/

Statements

Subject Item
wd:Q27677739
rdf:type
wikibase:Item
schema:description
Krankheit مرض يصيب الإنسان An osteogenesis imperfecta that is characterized by bone fragility and normal sclerae and has material basis in dominantly inherited mutations in the COL1A1 gene on chromosome 17q21.33 or the COL1A2 gene on chromosome 7q21.3. хвороба
p:P2888
wds:Q27677739-FDC36958-D0A4-43A3-B072-3BA944C0CE19 wds:Q27677739-FBD68989-AEFF-4C8E-9255-3443216F120A
wdt:P2888
n4:DOID_0110340 n12:0110340
p:P1995
wds:Q27677739-E33B0F5A-1679-44EE-A82B-A1A5967307A3
p:P5270
wds:Q27677739-6945C28A-7AFD-4CE3-8BF7-BC89D88CDDAA
p:P699
wds:Q27677739-13BA4EB4-7A6E-4FA7-B659-ADD75D369DC3
wdtn:P5270
n4:MONDO_0008148
wdtn:P699
n10:0110340
wdt:P1995
wd:Q1071953
wdt:P5270
MONDO_0008148
wdt:P699
DOID:0110340
rdfs:label
osteogenesis imperfecta type 4
skos:prefLabel
osteogenesis imperfecta type 4
schema:name
osteogenesis imperfecta type 4
p:P31
wds:Q27677739-2DF30C09-74FC-4871-B370-A3A9371D1DC8 wds:Q27677739-B42780A8-7837-46C0-A058-73E6DE0AF41D
wdt:P31
wd:Q112193867 wd:Q929833
p:P279
wds:Q27677739-B62C7738-11EC-465B-82AF-A078F94C24C8 wds:Q27677739-A72DD7EC-14DD-46A5-AC2B-1B76E066B67B wds:Q27677739-3600FD91-0BCA-4DCD-96DC-32AB507602EC
wdt:P279
wd:Q18553439 wd:Q749409 wd:Q200779
p:P11430
wds:Q27677739-cc9c6fdf-423f-0fe2-7ee0-ffc95d9a4bce
p:P1550
wds:Q27677739-c07c2f18-45fb-12e3-78e1-b13de6e752f7
p:P2293
wds:Q27677739-1B410D25-5093-4298-A71D-E649ECA56318 wds:Q27677739-FE3D36BB-32DF-496B-BF8F-7FC2EF7CBC01
p:P4229
wds:Q27677739-98ED4346-F4FD-4FE8-9AF3-AC6C187858DA
p:P4317
wds:Q27677739-67551E19-DC1E-401D-9A72-16D059DC0CC6
p:P492
wds:Q27677739-A7EB1DA6-7AA1-4F07-B741-E9C08C1724EF
wdt:P11430
DI-02103
wdt:P1550
216820
wdt:P2293
wd:Q14881725 wd:Q15317046
wdt:P4229
Q78.0
wdt:P4317
8696
wdt:P492
166220
skos:altLabel
osteogenesis imperfecta type IV OI4 osteogenesis imperfecta with normal sclera
p:P1748
wds:Q27677739-3b4cccb3-4c31-5e1b-7735-77f64b842b20
p:P5008
wds:Q27677739-FFEC45CE-1AF1-4565-8BAA-7FD98BDAE499
wdt:P1748
C98576
wdt:P5008
wd:Q4099686