SHMARQL
Docs
Query
Entity
Story editor
benign neonatal seizures
<http:/
/
www.wikidata.org/
entity/
Q15975183>
Human disease
rdfs:
label
ca
cy
en
es
fr
nn
"benign neonatal seizures"
@en
"benigne neonatale anfall"
@nn
"epilepsia benigna neonatal"
@es
"epilèpsia benigna neonatal"
@ca
"trawiadau newydd-anedig diniwed"
@cy
"épilepsie bénigne néonatale"
@fr
skos:
alt
Label
ca
en
es
nn
"BNS"
@nn
"Epilepsy, Benign Neonatal"
@en
"benign familial neonatal seizures"
@en
"benign neonatal convulsions"
@en
"epilepsia neonatal benigna"
@es
"epilèpsia neonatal benigna"
@ca
schema:
description
ar
de
en
hy
uk
"Human disease"
@en
"Krankheit"
@de
"хвороба людини"
@uk
"մարդու հիվանդություն"
@hy
"مرض يصيب الإنسان"
@ar
schema:
date
Modified
"2025-07-23T06:30:07+00:00"
^^xsd:dateTime
schema:
version
2382980719
wikibase:
identifiers
12
wikibase:
sitelinks
2
wikibase:
statements
24
p:
P1550
wd:
statement/Q15975183-76B6D5BC-FDEB-4B53-BF07-27A6A4910B6D
p:
P1748
wd:
statement/Q15975183-5B5349F5-3557-413D-BCE9-FDDD5F88FA59
p:
P1995
wd:
statement/Q15975183-1485535A-BAB8-4956-A125-C932F61CAE98
wd:
statement/Q15975183-8A1D9799-C8AC-49F0-843B-CF6F7FB8550C
p:
P2176
wd:
statement/Q15975183-4F0A466C-B106-4DAF-AC19-D117EF0ACC75
p:
P2293
wd:
statement/Q15975183-776624C3-81D1-4883-99D6-9254260E1C3A
wd:
statement/Q15975183-B93C4B05-2D41-4E5E-B207-76F772F621E5
p:
P279
wd:
statement/Q15975183-656751C0-632F-4866-AD88-6275F776736A
p:
P2888
wd:
statement/Q15975183-3A6F06FE-ADCE-4321-AD69-AA0BF6FC88A4
wd:
statement/Q15975183-6A3A8A02-9435-451D-99EA-211FE25B12F3
wd:
statement/Q15975183-90A2A12D-A0E7-4535-9E9F-0621B4D21E59
p:
P2892
wd:
statement/Q15975183-7ACB833B-CEEE-480D-AE8A-23E602BAE99E
wd:
statement/Q15975183-847E7B8C-4CBB-409E-9349-50B619C0A781
p:
P31
wd:
statement/Q15975183-7E1F3DD3-082C-44EB-A97B-1A8A7EEDAE5F
p:
P486
wd:
statement/Q15975183-68B2F2C2-1A1A-4C64-88C5-44C1BD20962C
p:
P492
wd:
statement/Q15975183-5578045B-C90E-4CFF-9DA9-B4908F0592CA
wd:
statement/Q15975183-8C69579E-657B-4C56-A2FB-6115F506BA5C
wd:
statement/Q15975183-C0DA05FE-F085-427E-BA24-7955046469D4
p:
P5008
wd:
statement/Q15975183-2E545A15-F56A-4EEF-B1BE-CC901E6B4193
p:
P6366
wd:
statement/Q15975183-B40B253D-F98F-470D-B044-ADDD58D2EE6E
p:
P672
wd:
statement/Q15975183-00469731-7040-4489-BFB5-55BAFA512995
wd:
statement/Q15975183-B2E0C63E-E838-4452-90AB-C9E467202E1E
p:
P699
wd:
statement/Q15975183-e4edaf3b-4707-15dd-cb91-b7325914ba0f
p:
P7464
wd:
statement/Q15975183-1407072D-7653-4991-B946-F79A99B62846
p:
direct-
normalized/
P486
<http:/
/
id.nlm.nih.gov/
mesh/
D020936>
p:
direct-
normalized/
P6366
<https:/
/
makg.org/
entity/
2776643595>
p:
direct-
normalized/
P672
<http:/
/
id.nlm.nih.gov/
mesh/
C10.228.140.490.370>
<http:/
/
id.nlm.nih.gov/
mesh/
C16.614.258>
p:
direct-
normalized/
P699
<http:/
/
purl.obolibrary.org/
obo/
DOID_DOID:14264>
wdt:
P1550
"1949"
wdt:
P1748
"C84593"
wdt:
P1995
pediatrics
neurology
wdt:
P2176
phenobarbital
wdt:
P2293
KCNQ2
KCNQ3
wdt:
P279
neonatal period electroclinical syndrome
wdt:
P2888
<http:/
/
identifiers.org/
doid/
DOID:14264>
<http:/
/
purl.obolibrary.org/
obo/
DOID_14264>
<http:/
/
www.orpha.net/
ORDO/
Orphanet_1949>
wdt:
P2892
"C0270851"
"C0393693"
wdt:
P31
type of disease
wdt:
P486
"D020936"
wdt:
P492
"121200"
"121201"
"269720"
wdt:
P5008
WikiProject Medicine
wdt:
P6366
"2776643595"
wdt:
P672
"C10.228.140.490.370"
"C16.614.258"
wdt:
P699
"DOID:14264"
wdt:
P7464
"benign-familial-neonatal-seizures"
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