PropertyValue
?:definition
  • Human SDHD wild-type allele is located in the vicinity of 11q23 and is approximately 33 kb in length. This allele, which encodes succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial protein, is involved in the localization of enzyme activity of the electron transport chain. Mutation of the gene is associated with hereditary paraganglioma type 1, pheochromocytoma, Carney-Stratakis syndrome and Cowden-like syndrome. Mutations also may be associated with intestinal carcinoid tumor.
?:hasCUIAnnotation
?:hasGeneratedBy
?:type

Metadata

Anon_0  
<http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://purl.org/net/provenance/ns#DataItem>
<http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://www.w3.org/2004/03/trix/rdfg-1/Graph>
<http://xmlns.com/foaf/0.1/primaryTopic> <https://research.tib.eu/covid-19/entity/C3273622_NCI>
<http://xmlns.com/foaf/0.1/topic> Anon_0
<http://www.ontologydesignpatterns.org/cp/owl/informationrealization.owl#realizes> <https://research.tib.eu/covid-19/data/entity/C3273622_NCI>
<http://purl.org/net/provenance/ns#createdBy>
Anon_1   (more)
expand all