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- NCIT_C199598 IAO_0000115 "A cytogenetic abnormality that refers to a chromosomal translocation that involves the long arm (q33.3) of chromosome 2 and the long arm (q12) of chromosome 22." @default.
- NCIT_C199598 NCIT_NHC0 "C199598" @default.
- NCIT_C199598 NCIT_P106 "Cell or Molecular Dysfunction" @default.
- NCIT_C199598 NCIT_P108 "t(2;22)(q33.3;q12)" @default.
- NCIT_C199598 NCIT_R173 NCIT_C12219 @default.
- NCIT_C199598 NCIT_R173 NCIT_C13202 @default.
- NCIT_C199598 NCIT_R173 NCIT_C13203 @default.
- NCIT_C199598 NCIT_R173 NCIT_C13215 @default.
- NCIT_C199598 NCIT_R173 NCIT_C13218 @default.
- NCIT_C199598 NCIT_R173 NCIT_C13404 @default.
- NCIT_C199598 NCIT_R173 NCIT_C14134 @default.
- NCIT_C199598 NCIT_R173 NCIT_C21599 @default.
- NCIT_C199598 normalizedInformationContent "100" @default.
- NCIT_C199598 referenceCount "1" @default.
- NCIT_C199598 hasExactSynonym "t(2;22)(q33.3;q12)" @default.
- NCIT_C199598 type Class @default.
- NCIT_C199598 isDefinedBy ncit.owl @default.
- NCIT_C199598 label "t(2;22)(q33.3;q12)" @default.
- NCIT_C199598 subClassOf B1d00df7007262c1a9d456505e1bc03a5 @default.
- NCIT_C199598 subClassOf B64d25fecc29e0a57096a57345a322376 @default.
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- NCIT_C199598 subClassOf B9c2182cd60e18fec96c2f84f35fac11b @default.
- NCIT_C199598 subClassOf NCIT_C199598 @default.
- NCIT_C199598 subClassOf NCIT_C2950 @default.
- NCIT_C199598 subClassOf NCIT_C3420 @default.
- NCIT_C199598 subClassOf NCIT_C36541 @default.
- NCIT_C199598 subClassOf NCIT_C3910 @default.