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- Ba92ed6044c1ae7b97abe8232ef5d2470 NCIT_P378 "NCI" @default.
- Ba92ed6044c1ae7b97abe8232ef5d2470 type Axiom @default.
- Ba92ed6044c1ae7b97abe8232ef5d2470 annotatedProperty IAO_0000115 @default.
- Ba92ed6044c1ae7b97abe8232ef5d2470 annotatedSource NCIT_C185487 @default.
- Ba92ed6044c1ae7b97abe8232ef5d2470 annotatedTarget "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.