|
rdfs:label
|
"Brugada syndrome 1"@en
"sindrom Brugada 1"@sl
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|
skos:altLabel
|
"BRGDA1"@en
|
|
"BRUGADA SYNDROME 1"@en
|
|
"BRUGADA SYNDROME 1; BRGDA1"@en
|
|
"Brugada Syndrome type 1"@en
|
|
"Cardiac Conduction Defect, Nonspecific"@en
|
|
"Right Bundle Branch Block, St Segment Elevation, and Sudden Death Syndrome"@en
|
|
"Sudden Unexplained Nocturnal Death Syndrome"@en
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|
schema:description
|
"Brugada syndrome that has material basis in heterozygous mutation in the SCN5A gene on chromosome 3p22"@en
"Krankheit"@de
"хвороба"@uk
"مرض يصيب الإنسان"@ar
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|
schema:dateModified
|
"2025-07-19T17:41:42+00:00"^^xsd:dateTime
|
|
schema:version
|
2381786780
|
|
wikibase:identifiers
|
8
|
|
wikibase:sitelinks
|
0
|
|
wikibase:statements
|
16
|
|
p:P11430
|
wd:statement/Q27677682-5b58e6dc-42f4-8368-e5c9-f4b18ad28e7d
|
|
p:P1995
|
wd:statement/Q27677682-21585861-2304-4B25-9838-BB44E39D2368
|
|
p:P2293
|
wd:statement/Q27677682-C024F5B7-CCFB-4706-8349-E851645B6B8A
|
|
p:P279
|
wd:statement/Q27677682-2DA8DC20-44AC-4DCF-AB08-41866F1C4152
|
|
wd:statement/Q27677682-A124A720-0101-4EDB-9FF2-1DEA9D7AD6DD
|
|
p:P2888
|
wd:statement/Q27677682-63BFD3F2-8220-4F91-A960-C6E1CAAB5991
|
|
wd:statement/Q27677682-DE307B67-738E-4DED-9ABB-AE0156EA0CC7
|
|
p:P2892
|
wd:statement/Q27677682-324D1F80-2A4E-4EEF-AA9E-C48AC4BA5194
|
|
wd:statement/Q27677682-3619B08F-7488-4C85-9CBC-3F171587241F
|
|
wd:statement/Q27677682-DF7ACB32-58F2-41D3-B3D1-C2A6E3822114
|
|
p:P31
|
wd:statement/Q27677682-25C0DD6B-BA55-4671-8F28-3F7F8E86AF8E
|
|
p:P4229
|
wd:statement/Q27677682-FC31251C-81F8-4130-917C-87A5C41FC336
|
|
p:P492
|
wd:statement/Q27677682-2357A168-F20C-4B7E-B5D5-3D2154BA7F6F
|
|
p:P5008
|
wd:statement/Q27677682-867FE209-3B86-4881-B9D9-C9019A32DD87
|
|
p:P5270
|
wd:statement/Q27677682-A6E41629-3A97-42D9-9B75-913D9C4AF7D1
|
|
p:P699
|
wd:statement/Q27677682-2EA63B65-C941-4361-BA63-4FE6D218B7D6
|
|
p:direct-normalized/P5270
|
<http://purl.obolibrary.org/obo/MONDO_0011001>
|
|
p:direct-normalized/P699
|
<http://purl.obolibrary.org/obo/DOID_DOID:0110218>
|
|
wdt:P11430
|
"DI-00202"
|
|
wdt:P1995
|
cardiology
|
|
wdt:P2293
|
SCN5A
|
|
wdt:P279
|
autosomal dominant disease
|
|
Brugada syndrome
|
|
wdt:P2888
|
<http://identifiers.org/doid/DOID:0110218>
|
|
<http://purl.obolibrary.org/obo/DOID_0110218>
|
|
wdt:P2892
|
"C1142166"
|
|
"C2748542"
|
|
"CN029323"
|
|
wdt:P31
|
type of disease
|
|
wdt:P4229
|
"I49.8"
|
|
wdt:P492
|
"601144"
|
|
wdt:P5008
|
WikiProject Medicine
|
|
wdt:P5270
|
"MONDO_0011001"
|
|
wdt:P699
|
"DOID:0110218"
|