SHMARQL
Docs
Query
Entity
Story editor
skin tumor or hamartoma
<http:/
/
www.wikidata.org/
entity/
Q55788604>
human disease
rdfs:
label
ca
en
fr
hi
pt
pt-br
ru
sl
"Tumor de pele, raro"
@pt
"Tumor de pele, raro"
@pt-br
"kožni tumor ali hamartom"
@sl
"skin tumor or hamartoma"
@en
"tumeur ou hamartome de la peau"
@fr
"tumor o hamartoma cutani"
@ca
"опухоль кожи или гамартома"
@ru
"त्वचा का ट्यूमर या हैमार्टोमा"
@hi
schema:
description
en
uk
"human disease"
@en
"хвороба людини"
@uk
schema:
date
Modified
"2026-10-24T00:36:25+00:00"
^^xsd:dateTime
schema:
version
2560167275
wikibase:
identifiers
4
wikibase:
sitelinks
0
wikibase:
statements
7
p:
P14914
wd:
statement/Q55788604-ED180403-4E6C-4CC4-A261-60F32A82EEB5
p:
P1550
wd:
statement/Q55788604-924C6E36-87F1-4514-BECF-6784F7D4C854
p:
P279
wd:
statement/Q55788604-F42B741A-F532-4753-B828-C52585B65ADF
p:
P2888
wd:
statement/Q55788604-4A254B5A-F547-4CE0-9565-47AEAE52D2E6
p:
P2892
wd:
statement/Q55788604-9B24724E-DBD1-48ED-A82E-899AEE85BE1D
p:
P31
wd:
statement/Q55788604-6B3B10D3-A061-4E14-A16C-493809BEF453
p:
P5270
wd:
statement/Q55788604-23D21BD7-284E-4BA3-BDCB-AFA2A7DDBF5F
p:
direct-
normalized/
P5270
<http:/
/
purl.obolibrary.org/
obo/
MONDO_0019300>
wdt:
P14914
"D79386"
wdt:
P1550
"79386"
wdt:
P279
inherited skin tumor
wdt:
P2888
<http:/
/
www.orpha.net/
ORDO/
Orphanet_79386>
wdt:
P2892
"C5681474"
wdt:
P31
type of disease
wdt:
P5270
"MONDO_0019300"
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data from SPARQL profile:
Wikidata