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- NCIT_C185487 IAO_0000115 "An indication that the RTK1-type molecular signature for pediatric high grade glioma was detected in a sample. This signature occurs more frequently in supratentorial than infratentorial gliomas and co-occurs with expression of both wild-type histone H3 and wild-type IDH. The RTK1-type molecular signature is characterized by the following molecular abnormalities (in order of most to least frequent) TP53 gene mutation, PDGFRA gene amplification, homozygous deletion of chromosome 9p, MGMT promoter methylation and loss of ATRX protein expression. This signature may rarely include gain of chromosome 7, loss of chromosome 10q, CDK4/6 mutations and MYCN gene amplification. Additionally, EGFR gene amplification and TERT promoter mutation are not characteristics of this signature." @default.
- NCIT_C185487 NCIT_NHC0 "C185487" @default.
- NCIT_C185487 NCIT_P106 "Laboratory or Test Result" @default.
- NCIT_C185487 NCIT_P108 "Pediatric Glioma RTK1 Molecular Signature Detected" @default.
- NCIT_C185487 NCIT_P171 "28401334" @default.
- NCIT_C185487 NCIT_P208 "CL1773677" @default.
- NCIT_C185487 normalizedInformationContent "95.413332725061409" @default.
- NCIT_C185487 referenceCount "2" @default.
- NCIT_C185487 hasExactSynonym "Pediatric Glioma RTK1 Molecular Signature Detected" @default.
- NCIT_C185487 hasExactSynonym "pedGBM_RTK1 Signature Detected" @default.
- NCIT_C185487 type Class @default.
- NCIT_C185487 isDefinedBy ncit.owl @default.
- NCIT_C185487 label "Pediatric Glioma RTK1 Molecular Signature Detected" @default.
- NCIT_C185487 subClassOf NCIT_C150123 @default.
- NCIT_C185487 subClassOf NCIT_C185487 @default.
- NCIT_C185487 subClassOf NCIT_C3367 @default.
- NCIT_C185487 subClassOf NCIT_C35682 @default.
- NCIT_C185487 subClassOf NCIT_C36292 @default.
- NCIT_C185487 subClassOf NCIT_C7057 @default.
- NCIT_C185487 subClassOf NCIT_C77140 @default.