SHMARQL

OMIM ID

<http://www.wikidata.org/entity/P492>

wikibase:Property
Online "Mendelian Inheritance in Man" catalogue codes for diseases, genes, or phenotypes
rdfs:label
"OMIM ID"@en
skos:altLabel
"MIM number"@en
"OMIM"@en
"Online Mendelian Inheritance in Man"@en
schema:description
"Online "Mendelian Inheritance in Man" catalogue codes for diseases, genes, or phenotypes"@en
schema:dateModified "2026-02-17T17:25:25+00:00"^^xsd:dateTime
schema:version 2464202799
wikibase:claim p:P492
wikibase:directClaim wdt:P492
wikibase:directClaimNormalized p:direct-normalized/P492
wikibase:novalue p:novalue/P492
wikibase:propertyType wikibase:ExternalId
wikibase:qualifier p:qualifier/P492
wikibase:qualifierValue p:qualifier/value/P492
wikibase:qualifierValueNormalized p:qualifier/value-normalized/P492
wikibase:reference p:reference/P492
wikibase:referenceValue p:reference/value/P492
wikibase:referenceValueNormalized p:reference/value-normalized/P492
wikibase:statementProperty p:statement/P492
wikibase:statementValue p:statement/value/P492
wikibase:statementValueNormalized p:statement/value-normalized/P492
wikibase:statements 23
p:P1552 wd:statement/P492-683F82DA-7736-4E10-B56C-D6CDFB01659C
p:P1629 wd:statement/P492-4c5a9de1-471a-dea1-ce74-ab1706aea1d6
wd:statement/P492-aa562343-49d6-f526-0025-3a4c260d5c9b
wd:statement/P492-d7c7cb89-4049-135c-f98d-675d3479e070
p:P1630 wd:statement/P492-527CB1DC-3EE1-40FB-B737-C4460BD8C688
wd:statement/P492-cb297386-4ca6-a960-ead0-f7d034102638
p:P1793 wd:statement/P492-3f3e530e-430b-fe17-c52e-84f9bffb1133
p:P1855 wd:statement/P492-bd58faaf-4e07-e18a-44bb-6f62c6832140
wd:statement/P492-c591a6fe-4bd5-9756-5cb9-13b1d7c4f56c
p:P2302 wd:statement/P492-3F9C7483-8625-40FA-B204-13BCC42A7206
wd:statement/P492-A59C03AC-A5EB-4737-AD8D-DC411DFE7F0B
wd:statement/P492-D2FD9B4F-C3AD-4DAF-887B-1BDB20E96B4D
wd:statement/P492-EE426807-E5A9-4E50-8ED9-91A20B98305F
p:P2378 wd:statement/P492-95ee0204-423a-5c47-f480-31a71792cd2e
p:P2875 wd:statement/P492-31E95B85-1559-4B06-ACEE-6AA8E81CA89D
p:P31 wd:statement/P492-2e89a03d-4d82-e5fd-fd8d-342ee43ddf4f
wd:statement/P492-430397AE-AF1A-475C-8094-6E4F4D76D3E1
p:P3254 wd:statement/P492-77250334-EBBC-4901-A9BB-D461A0C666C9
p:P3713 wd:statement/P492-fcc86584-42de-3aa7-d411-d35c405d0867
p:P4354 wd:statement/P492-6ec7f825-4a28-b36d-03e2-2db65d1d39eb
p:P4876 wd:statement/P492-faff94e0-4509-bc3b-8657-b6463165fd4a
p:P8966 wd:statement/P492-1d4f384c-44fe-3139-72dc-046abdcaa112
p:P9073 wd:statement/P492-E04BDCAE-2159-45CB-ABA4-7F90723EE7F6
wdt:P1552 numeric identifier
wdt:P1629 phenotype
disease
gene
wdt:P1630 "https://omim.org/OMIM:$1"
"https://omim.org/entry/$1"
wdt:P1793 "\d{6}"
wdt:P1855 Huntington's disease
dengue fever
wdt:P2302 format constraint
subject type constraint
allowed-entity-types constraint
property scope constraint
wdt:P2378 Online Mendelian Inheritance in Man
wdt:P2875 Category:Pages using Wikidata property P492
wdt:P31 Wikidata property related to medicine
Wikidata property to identify genes
wdt:P3254 <https://www.wikidata.org/wiki/Wikidata:Property_proposal/Archive/7#P492>
wdt:P3713 Category:P492 not in Wikidata
wdt:P4354 "https://omim.org/search?index=entry&start=1&search=$1&sort=score+desc%2C+prefix_sort+desc&limit=10&field=number"
wdt:P4876 27073.0^^xsd:decimal
wdt:P8966 "^https?:\/\/omim\.org\/entry\/(\d{6})"
wdt:P9073 Online Mendelian Inheritance in Man
Download as:
TurtleJSON-LDRDF/XML
data from SPARQL profile: Wikidata