Matches in Ubergraph for { <http://purl.obolibrary.org/obo/NCIT_C84734> ?p ?o ?g. }
Showing items 1 to 24 of
24
with 100 items per page.
- NCIT_C84734 IAO_0000115 "An autosomal recessive inherited type of glycogen storage disease caused by deficiency of the enzyme acid alpha-glucosidase. It results in the abnormal accumulation of glycogen in the heart, skeletal muscles, liver, and nervous system." @default.
- NCIT_C84734 NCIT_NHC0 "C84734" @default.
- NCIT_C84734 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C84734 NCIT_P108 "Glycogen Storage Disease Type II" @default.
- NCIT_C84734 NCIT_P207 "C0017921" @default.
- NCIT_C84734 NCIT_P322 "Cellosaurus" @default.
- NCIT_C84734 normalizedInformationContent "95.413332725061409" @default.
- NCIT_C84734 referenceCount "2" @default.
- NCIT_C84734 hasExactSynonym "Glycogen Storage Disease Type II" @default.
- NCIT_C84734 inSubset NCIT_C165258 @default.
- NCIT_C84734 inSubset NCIT_C192842 @default.
- NCIT_C84734 type Class @default.
- NCIT_C84734 isDefinedBy ncit.owl @default.
- NCIT_C84734 label "Glycogen Storage Disease Type II" @default.
- NCIT_C84734 subClassOf NCIT_C2991 @default.
- NCIT_C84734 subClassOf NCIT_C3235 @default.
- NCIT_C84734 subClassOf NCIT_C34816 @default.
- NCIT_C84734 subClassOf NCIT_C4873 @default.
- NCIT_C84734 subClassOf NCIT_C53529 @default.
- NCIT_C84734 subClassOf NCIT_C53543 @default.
- NCIT_C84734 subClassOf NCIT_C53547 @default.
- NCIT_C84734 subClassOf NCIT_C61272 @default.
- NCIT_C84734 subClassOf NCIT_C7057 @default.
- NCIT_C84734 subClassOf NCIT_C84734 @default.