About: gene mutation

Facets (new session)
Description
Metadata
Settings
- owl:sameAs
- Inference Rule:

About: gene mutation Goto Sponge NotDistinct Permalink

An Entity of Type : http://wikiba.se/ontology#Item, within Data Space : covidontheweb.inria.fr associated with source document(s)

Attributes	Values
type	Item
label	gene mutation single gene mutation
preferred label	single gene mutation
described by	https://covidontheweb.inria.fr:4443/about/id/entity/http/ns.inria.fr/covid19/graph/wikidata-named-entities-full proxy:entity/http/ns.inria.fr/covid19/graph/wikidata-named-entities-full https://covidontheweb.inria.fr:4443/about/id/entity/http/www.wikidata.org/entity/Q1415380
schema:name	single gene mutation
schema:description	mutation in just one gene
is wdt:P279 of	insertion mutation trichorhinophalangeal syndrome type II Nonsense mutation chromosome 1q21.1 deletion syndrome silent mutation DiGeorge syndrome point mutation missense mutation deletion mutation Wolf-Hirschhorn syndrome WAGR syndrome chromosome 1p36 deletion syndrome Williams-Beuren syndrome 22q13 deletion syndrome hereditary neuropathy with liability to pressure palsies chromosome 3q29 microdeletion syndrome Smith-Magenis syndrome chromosome 18q deletion syndrome
is topic of	point mutation covid:graph/wikidata-named-entities-full
is http://www.wikidat...op/statement/P279 of	wd:statement/Q1415380-59328bb9-4851-5cf1-0208-aa40ca3a3498

Faceted Search & Find service v1.13.91 as of Mar 24 2020

Alternative Linked Data Documents: Sponger | ODE Content Formats:

RDF

ODATA

Microdata

About

OpenLink Virtuoso version 07.20.3229 as of Jul 10 2020, on Linux (x86_64-pc-linux-gnu), Single-Server Edition (94 GB total memory)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2024 OpenLink Software