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- NCIT_C120408 IAO_0000115 "A microdeletion at 16p11.2, characterized by a predisposition to obesity, developmental delay and autism spectrum disorders." @default.
- NCIT_C120408 NCIT_NHC0 "C120408" @default.
- NCIT_C120408 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C120408 NCIT_P108 "Chromosome 16p11.2 Deletion Syndrome" @default.
- NCIT_C120408 NCIT_P207 "C3697355" @default.
- NCIT_C120408 NCIT_P322 "Cellosaurus" @default.
- NCIT_C120408 NCIT_P322 "NICHD" @default.
- NCIT_C120408 NCIT_P325 "A microdeletion at 16p11.2, characterized by a predisposition to obesity, developmental delay, and autism spectrum conditions." @default.
- NCIT_C120408 NCIT_R174 NCIT_C12219 @default.
- NCIT_C120408 NCIT_R174 NCIT_C13202 @default.
- NCIT_C120408 NCIT_R174 NCIT_C13203 @default.
- NCIT_C120408 NCIT_R174 NCIT_C13211 @default.
- NCIT_C120408 NCIT_R174 NCIT_C13404 @default.
- NCIT_C120408 NCIT_R174 NCIT_C14134 @default.
- NCIT_C120408 NCIT_R174 NCIT_C21599 @default.
- NCIT_C120408 normalizedInformationContent "100" @default.
- NCIT_C120408 referenceCount "1" @default.
- NCIT_C120408 hasExactSynonym "Chromosome 16p11.2 Deletion Syndrome" @default.
- NCIT_C120408 inSubset NCIT_C118467 @default.
- NCIT_C120408 inSubset NCIT_C165258 @default.
- NCIT_C120408 inSubset NCIT_C192842 @default.
- NCIT_C120408 inSubset NCIT_C90259 @default.
- NCIT_C120408 type Class @default.
- NCIT_C120408 isDefinedBy ncit.owl @default.
- NCIT_C120408 label "Chromosome 16p11.2 Deletion Syndrome" @default.
- NCIT_C120408 subClassOf B2d81f37f31e103535401ed7b16409c41 @default.
- NCIT_C120408 subClassOf Bea21809f57dcfd2092ff1ad3d052e66d @default.
- NCIT_C120408 subClassOf NCIT_C120408 @default.
- NCIT_C120408 subClassOf NCIT_C28193 @default.
- NCIT_C120408 subClassOf NCIT_C2991 @default.
- NCIT_C120408 subClassOf NCIT_C7057 @default.