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- NCIT_C185486 IAO_0000115 "An indication that the MYCN-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 MYCN-type molecular signature is characterized by the following molecular abnormalities (in order of most to least frequent) TP53 gene mutations, MYCN gene amplification, gain of chromosome 7, loss of chromosome 10q, TERT promoter mutation, EGFR gene amplification and CDK4/6 mutations. This signature may rarely include MGMT promoter methylation, homozygous deletion of chromosome 9p. PDGFRA gene amplification and loss of ATRX protein expression." @default.
- NCIT_C185486 NCIT_NHC0 "C185486" @default.
- NCIT_C185486 NCIT_P106 "Laboratory or Test Result" @default.
- NCIT_C185486 NCIT_P108 "Pediatric Glioma MYCN Molecular Signature Detected" @default.
- NCIT_C185486 NCIT_P171 "28401334" @default.
- NCIT_C185486 NCIT_P208 "CL1773676" @default.
- NCIT_C185486 normalizedInformationContent "95.413332725061409" @default.
- NCIT_C185486 referenceCount "2" @default.
- NCIT_C185486 hasExactSynonym "Pediatric Glioma MYCN Molecular Signature Detected" @default.
- NCIT_C185486 hasExactSynonym "pedGBM_MYCN Signature Detected" @default.
- NCIT_C185486 type Class @default.
- NCIT_C185486 isDefinedBy ncit.owl @default.
- NCIT_C185486 label "Pediatric Glioma MYCN Molecular Signature Detected" @default.
- NCIT_C185486 subClassOf NCIT_C150123 @default.
- NCIT_C185486 subClassOf NCIT_C185486 @default.
- NCIT_C185486 subClassOf NCIT_C3367 @default.
- NCIT_C185486 subClassOf NCIT_C35682 @default.
- NCIT_C185486 subClassOf NCIT_C36292 @default.
- NCIT_C185486 subClassOf NCIT_C7057 @default.
- NCIT_C185486 subClassOf NCIT_C77140 @default.