Matches in Ubergraph for { <http://purl.obolibrary.org/obo/NCIT_C185488> ?p ?o ?g. }
Showing items 1 to 20 of
20
with 100 items per page.
- NCIT_C185488 IAO_0000115 "An indication that the RTK2-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 RTK2-type molecular signature is characterized by the following molecular abnormalities (in order of most to least frequent) homozygous deletion of chromosome 9p, TERT promoter mutation, EGFR gene amplification, TP53 gene mutation, loss of chromosome 10q, gain of chromosome 7 and CDK4/6 mutations. This signature may rarely include MYCN gene amplification and PDGFRA gene amplification. Additionally, MGMT promoter methylation and loss of ATRX protein expression are not characteristics of this signature." @default.
- NCIT_C185488 NCIT_NHC0 "C185488" @default.
- NCIT_C185488 NCIT_P106 "Laboratory or Test Result" @default.
- NCIT_C185488 NCIT_P108 "Pediatric Glioma RTK2 Molecular Signature Detected" @default.
- NCIT_C185488 NCIT_P171 "28401334" @default.
- NCIT_C185488 NCIT_P208 "CL1773682" @default.
- NCIT_C185488 normalizedInformationContent "95.413332725061409" @default.
- NCIT_C185488 referenceCount "2" @default.
- NCIT_C185488 hasExactSynonym "Pediatric Glioma RTK2 Molecular Signature Detected" @default.
- NCIT_C185488 hasExactSynonym "pedGBM_RTK2 Signature Detected" @default.
- NCIT_C185488 type Class @default.
- NCIT_C185488 isDefinedBy ncit.owl @default.
- NCIT_C185488 label "Pediatric Glioma RTK2 Molecular Signature Detected" @default.
- NCIT_C185488 subClassOf NCIT_C150123 @default.
- NCIT_C185488 subClassOf NCIT_C185488 @default.
- NCIT_C185488 subClassOf NCIT_C3367 @default.
- NCIT_C185488 subClassOf NCIT_C35682 @default.
- NCIT_C185488 subClassOf NCIT_C36292 @default.
- NCIT_C185488 subClassOf NCIT_C7057 @default.
- NCIT_C185488 subClassOf NCIT_C77140 @default.