About: syndromic neurometabolic disease with non-X-linked intellectual disability

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

About: syndromic neurometabolic disease with non-X-linked intellectual disability Goto Sponge NotDistinct Permalink

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

Attributes	Values
type	Item
label	syndromic neurometabolic disease with non-X-linked intellectual disability
preferred label	syndromic neurometabolic disease with non-X-linked intellectual disability
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 proxy:entity/http/www.wikidata.org/entity/Q998273 https://covidontheweb.inria.fr:4443/about/id/entity/http/www.wikidata.org/entity/Q998273
schema:name	syndromic neurometabolic disease with non-X-linked intellectual disability
schema:description	human disease
is wdt:P279 of	Peters plus syndrome Smith-Lemli-Opitz syndrome congenital disorder of glycosylation type IIc guanidinoacetate methyltransferase deficiency
is topic of	Smith-Lemli-Opitz syndrome covid:graph/wikidata-named-entities-full
is http://www.wikidat...op/statement/P279 of	wd:statement/Q998273-73E55C81-A669-4DC8-896A-E81A99A3A090

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