Matches in Ubergraph for { <http://purl.obolibrary.org/obo/NCIT_C81315> ?p ?o ?g. }
Showing items 1 to 29 of
29
with 100 items per page.
- NCIT_C81315 IAO_0000115 "An autonomic recessive genetic disorder characterized by the body's inability to metabolize and utilize the amino acid phenylalanine, resulting in mental retardation, behavioral and movement problems, seizures, and developmental delays." @default.
- NCIT_C81315 NCIT_NHC0 "C81315" @default.
- NCIT_C81315 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C81315 NCIT_P108 "Phenylketonuria" @default.
- NCIT_C81315 NCIT_P207 "C0031485" @default.
- NCIT_C81315 NCIT_P322 "Cellosaurus" @default.
- NCIT_C81315 NCIT_P322 "NICHD" @default.
- NCIT_C81315 NCIT_P325 "An inherited disorder that causes a build-up of phenylalanine (an amino acid) in the blood. This can cause mental retardation, behavioral and movement problems, seizures, and delayed development. Using a blood test, PKU can easily be found in newborns, and treatment is a diet low in phenylalanine." @default.
- NCIT_C81315 NCIT_P366 "Phenylketonuria" @default.
- NCIT_C81315 normalizedInformationContent "89.350088392419622" @default.
- NCIT_C81315 referenceCount "5" @default.
- NCIT_C81315 hasExactSynonym "PKU" @default.
- NCIT_C81315 hasExactSynonym "Phenylketonuria" @default.
- NCIT_C81315 hasExactSynonym "phenylketonuria" @default.
- NCIT_C81315 inSubset NCIT_C165258 @default.
- NCIT_C81315 inSubset NCIT_C192842 @default.
- NCIT_C81315 inSubset NCIT_C89506 @default.
- NCIT_C81315 inSubset NCIT_C90259 @default.
- NCIT_C81315 type Class @default.
- NCIT_C81315 isDefinedBy ncit.owl @default.
- NCIT_C81315 label "Phenylketonuria" @default.
- NCIT_C81315 subClassOf NCIT_C2991 @default.
- NCIT_C81315 subClassOf NCIT_C3235 @default.
- NCIT_C81315 subClassOf NCIT_C34816 @default.
- NCIT_C81315 subClassOf NCIT_C53529 @default.
- NCIT_C81315 subClassOf NCIT_C53547 @default.
- NCIT_C81315 subClassOf NCIT_C7057 @default.
- NCIT_C81315 subClassOf NCIT_C81315 @default.
- NCIT_C81315 subClassOf NCIT_C97090 @default.