DOID:0081278

• Ontology
• Class
  • owl:Thing
    • host health status
      • disease
        • additional diseases by category
          • disease of anatomical entity
            • nervous system disease
              • central nervous system disease
                • central nervous system cancer
                  • malignant astrocytoma
                    • infant-type hemispheric glioma
              • nervous system cancer
                • central nervous system cancer
                  • malignant astrocytoma
                    • infant-type hemispheric glioma
        • neoplasm
          • cancer
            • cell type cancer
              • high grade glioma
                • malignant astrocytoma
                  • infant-type hemispheric glioma
            • organ system cancer
              • nervous system cancer
                • central nervous system cancer
                  • malignant astrocytoma
                    • infant-type hemispheric glioma
• Annotation Property
• Data Property
• Object Property
• Individual
• Datatype

• label
  • infant-type hemispheric glioma ^@en
• definition
  • A malignant astrocytoma that is characterized by receptor tyrosine kinase fusions in the NTRK family, ROS1, ALK, or MET genes, that arises in the cerebral hemisphere and occurs in early childhood. ^xsd:string
    • oio:hasDbXref
      • url:https://pubmed.ncbi.nlm.nih.gov/35404193/ ^xsd:string
      • url:https://pubmed.ncbi.nlm.nih.gov/36315913/ ^xsd:string
      • url:https://pubmed.ncbi.nlm.nih.gov/36316040/ ^xsd:string
• has_obo_namespace
  • disease_ontology ^xsd:string
• id
  • DOID:0081278 ^xsd:string
• oio:hasDbXref
  • NCI:C185471 ^xsd:string
  • ICDO:9385/3 ^xsd:string
• rdf:type
  • owl:Class
• rdfs:subClassOf
  • malignant astrocytoma