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- NCIT_C177544 IAO_0000115 "An X-linked genetic condition caused by duplication of a small segment of Xq25, which may encompass the GRIA3 and STAG2 genes, encoding glutamate receptor 3 and cohesin subunit SA-2. It is characterized by intellectual disability and distinctive facial dysmorphisms." @default.
- NCIT_C177544 NCIT_NHC0 "C177544" @default.
- NCIT_C177544 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C177544 NCIT_P108 "Xq25 Microduplication Syndrome" @default.
- NCIT_C177544 NCIT_P208 "CL1643199" @default.
- NCIT_C177544 NCIT_P322 "Cellosaurus" @default.
- NCIT_C177544 NCIT_R174 NCIT_C12219 @default.
- NCIT_C177544 NCIT_R174 NCIT_C13202 @default.
- NCIT_C177544 NCIT_R174 NCIT_C13203 @default.
- NCIT_C177544 NCIT_R174 NCIT_C13285 @default.
- NCIT_C177544 NCIT_R174 NCIT_C13404 @default.
- NCIT_C177544 NCIT_R174 NCIT_C14134 @default.
- NCIT_C177544 NCIT_R174 NCIT_C21599 @default.
- NCIT_C177544 normalizedInformationContent "100" @default.
- NCIT_C177544 referenceCount "1" @default.
- NCIT_C177544 hasExactSynonym "Xq25 Microduplication Syndrome" @default.
- NCIT_C177544 inSubset NCIT_C165258 @default.
- NCIT_C177544 inSubset NCIT_C192842 @default.
- NCIT_C177544 type Class @default.
- NCIT_C177544 isDefinedBy ncit.owl @default.
- NCIT_C177544 label "Xq25 Microduplication Syndrome" @default.
- NCIT_C177544 subClassOf Be38ef3e0bd336471817df430da6f56d5 @default.
- NCIT_C177544 subClassOf Bff5898d41efff28df72a07d93b72f942 @default.
- NCIT_C177544 subClassOf NCIT_C177544 @default.
- NCIT_C177544 subClassOf NCIT_C28193 @default.
- NCIT_C177544 subClassOf NCIT_C2991 @default.
- NCIT_C177544 subClassOf NCIT_C7057 @default.