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- NCIT_C75456 IAO_0000115 "A very rare genetic syndrome caused by deletions on the proximal short arm of chromosome 11. It is characterized by the presence of multiple exostoses and enlarged parietal foramina." @default.
- NCIT_C75456 NCIT_NHC0 "C75456" @default.
- NCIT_C75456 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C75456 NCIT_P108 "Potocki-Shaffer Syndrome" @default.
- NCIT_C75456 NCIT_P207 "C1832588" @default.
- NCIT_C75456 NCIT_P322 "Cellosaurus" @default.
- NCIT_C75456 NCIT_P366 "Potocki_Shaffer_Syndrome" @default.
- NCIT_C75456 NCIT_R174 NCIT_C12219 @default.
- NCIT_C75456 NCIT_R174 NCIT_C13202 @default.
- NCIT_C75456 NCIT_R174 NCIT_C13203 @default.
- NCIT_C75456 NCIT_R174 NCIT_C13206 @default.
- NCIT_C75456 NCIT_R174 NCIT_C13404 @default.
- NCIT_C75456 NCIT_R174 NCIT_C14134 @default.
- NCIT_C75456 NCIT_R174 NCIT_C21599 @default.
- NCIT_C75456 normalizedInformationContent "100" @default.
- NCIT_C75456 referenceCount "1" @default.
- NCIT_C75456 hasExactSynonym "Potocki-Shaffer Syndrome" @default.
- NCIT_C75456 inSubset NCIT_C165258 @default.
- NCIT_C75456 inSubset NCIT_C192842 @default.
- NCIT_C75456 type Class @default.
- NCIT_C75456 isDefinedBy ncit.owl @default.
- NCIT_C75456 label "Potocki-Shaffer Syndrome" @default.
- NCIT_C75456 subClassOf B425423994d6bc08b1302745c20fed823 @default.
- NCIT_C75456 subClassOf Ba49d9d3172b4fc88e14d64384ded5bb7 @default.
- NCIT_C75456 subClassOf NCIT_C28193 @default.
- NCIT_C75456 subClassOf NCIT_C2991 @default.
- NCIT_C75456 subClassOf NCIT_C4873 @default.
- NCIT_C75456 subClassOf NCIT_C53529 @default.
- NCIT_C75456 subClassOf NCIT_C53543 @default.
- NCIT_C75456 subClassOf NCIT_C53547 @default.
- NCIT_C75456 subClassOf NCIT_C7057 @default.
- NCIT_C75456 subClassOf NCIT_C75456 @default.