About: BRCA2 Syndrome     Goto   Sponge   Distinct   Permalink

An Entity of Type : owl:Class, within Data Space : linked.opendata.cz associated with source document(s)

AttributesValues
rdf:type
rdfs:label
  • BRCA2 Syndrome
equivalentClass
Semantic_Type
  • Disease or Syndrome
Preferred_Name
  • BRCA2 Syndrome
UMLS_CUI
  • C1332443
Legacy_Concept_Name
  • BRCA_2_Syndrome
FULL_SYN
  • BRCA2 SyndromePTNCI
  • Site Specific Early Onset Breast Cancer SyndromeSYNCI
DEFINITION
  • An autosomal dominant inherited syndrome caused by mutations in the BRCA2 gene. Patients are at high risk of developing female and male breast cancer, ovarian cancer, and other cancers including prostatic cancer, pancreatic cancer, gastric cancer, and melanoma.NCI
code
  • C36101
is someValuesFrom of
Faceted Search & Find service v1.16.118 as of Jun 21 2024


Alternative Linked Data Documents: 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 07.20.3240 as of Jun 21 2024, on Linux (x86_64-pc-linux-gnu), Single-Server Edition (126 GB total memory, 18 GB memory in use)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2024 OpenLink Software