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- NCIT_C179298 IAO_0000115 "A genetic condition caused by mutation(s) in the PRKG2 gene, encoding cGMP-dependent protein kinase 2. It is characterized by acromelia and mesomelia." @default.
- NCIT_C179298 NCIT_NHC0 "C179298" @default.
- NCIT_C179298 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C179298 NCIT_P108 "Acromesomelic Dysplasia, PRKG2 Type" @default.
- NCIT_C179298 NCIT_P208 "CL1661879" @default.
- NCIT_C179298 NCIT_P322 "Cellosaurus" @default.
- NCIT_C179298 NCIT_R176 NCIT_C16612 @default.
- NCIT_C179298 NCIT_R176 NCIT_C21281 @default.
- NCIT_C179298 NCIT_R176 NCIT_C24695 @default.
- NCIT_C179298 NCIT_R176 NCIT_C25870 @default.
- NCIT_C179298 NCIT_R176 NCIT_C25871 @default.
- NCIT_C179298 NCIT_R176 NCIT_C25872 @default.
- NCIT_C179298 NCIT_R176 NCIT_C25873 @default.
- NCIT_C179298 normalizedInformationContent "100" @default.
- NCIT_C179298 referenceCount "1" @default.
- NCIT_C179298 hasExactSynonym "AMDP" @default.
- NCIT_C179298 hasExactSynonym "Acromesomelic Dysplasia, PRKG2 Type" @default.
- NCIT_C179298 inSubset NCIT_C165258 @default.
- NCIT_C179298 inSubset NCIT_C192842 @default.
- NCIT_C179298 type Class @default.
- NCIT_C179298 isDefinedBy ncit.owl @default.
- NCIT_C179298 label "Acromesomelic Dysplasia, PRKG2 Type" @default.
- NCIT_C179298 subClassOf B1d28b19eedff9de8a683a090d097e259 @default.
- NCIT_C179298 subClassOf Bcb2f31394c2273ecb084b0e9a81036fe @default.
- NCIT_C179298 subClassOf NCIT_C179298 @default.
- NCIT_C179298 subClassOf NCIT_C2991 @default.
- NCIT_C179298 subClassOf NCIT_C4873 @default.
- NCIT_C179298 subClassOf NCIT_C53529 @default.
- NCIT_C179298 subClassOf NCIT_C53543 @default.
- NCIT_C179298 subClassOf NCIT_C53547 @default.
- NCIT_C179298 subClassOf NCIT_C7057 @default.