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- NCIT_C129355 IAO_0000115 "A cytogenetic abnormality characterized by the occurrence of a large number of chromosomal rearrangements that are restricted to sites in one or a few chromosomes. Chromothripsis may result from a single catastrophic event that causes multiple double-strand breaks, which are subsequently repaired or reassembled by error-prone DNA repair pathways or through aberrant DNA replication mechanisms." @default.
- NCIT_C129355 NCIT_NHC0 "C129355" @default.
- NCIT_C129355 NCIT_P106 "Cell or Molecular Dysfunction" @default.
- NCIT_C129355 NCIT_P108 "Chromothripsis" @default.
- NCIT_C129355 NCIT_P171 "26455580" @default.
- NCIT_C129355 NCIT_P207 "C4277538" @default.
- NCIT_C129355 normalizedInformationContent "100" @default.
- NCIT_C129355 referenceCount "1" @default.
- NCIT_C129355 hasExactSynonym "Chromothripsis" @default.
- NCIT_C129355 type Class @default.
- NCIT_C129355 isDefinedBy ncit.owl @default.
- NCIT_C129355 label "Chromothripsis" @default.
- NCIT_C129355 subClassOf NCIT_C129355 @default.
- NCIT_C129355 subClassOf NCIT_C2950 @default.
- NCIT_C129355 subClassOf NCIT_C3910 @default.