Not logged in : Login
(Sponging disallowed)

About: nodeID://b50941009       Sponge   NotDistinct   Permalink

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

AttributesValues
type
described by
Type
annotatedProperty
annotatedSource
annotatedTarget
  • A developmental and epileptic encephalopathy characterized by onset of seizures in infancy or early childhood, global developmental delay and variable intellectual disability that has_material_basis_in heterozygous mutation in the GABRB2 gene on chromosome 5q34.
database_cross_reference
  • url:https://www.ncbi.nlm.nih.gov/pubmed/25124326
  • url:https://www.ncbi.nlm.nih.gov/pubmed/29100083
is topic of
Faceted Search & Find service v1.17_git150 as of Jan 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, 67 GB memory in use)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2025 OpenLink Software