Not logged in : Login
(Sponging disallowed)

About: cone dystrophy     Goto   Sponge   NotDistinct   Permalink

An Entity of Type : owl:Class, within Data Space : linkeddata.uriburner.com:28898 associated with source document(s)

AttributesValues
type
subClassOf
label
  • cone dystrophy
has exact match
  • MESH:D000077765
described by
id
  • DOID:0050795
created_by
  • lschriml
creation_date
  • 2013-11-12T01:19:22Z
database_cross_reference
  • GARD:11897
  • MESH:D000077765
has_exact_synonym
  • retinal cone dystrophy (en)
has_obo_namespace
  • disease_ontology
http://purl.obolib...g/obo/IAO_0000115
  • A retinal disease that is characterized by the loss of cone cells, the photoreceptors responsible for both central and color vision.
is subClassOf of
is topic of
is annotatedSource of
Faceted Search & Find service v1.17_git151 as of Feb 20 2025


Alternative Linked Data Documents: iSPARQL | ODE     Content Formats:   [cxml] [csv]     RDF   [text] [turtle] [ld+json] [rdf+json] [rdf+xml]     ODATA   [atom+xml] [odata+json]     Microdata   [microdata+json] [html]    About   
This material is Open Knowledge   W3C Semantic Web Technology [RDF Data] Valid XHTML + RDFa
OpenLink Virtuoso version 08.03.3332 as of Jan 29 2025, on Linux (x86_64-generic-linux-glibc25), Single-Server Edition (378 GB total memory, 79 GB memory in use)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2025 OpenLink Software