Matches in Ubergraph for { <http://purl.obolibrary.org/obo/NCIT_C176014> ?p ?o ?g. }
Showing items 1 to 30 of
30
with 100 items per page.
- NCIT_C176014 IAO_0000115 "An autosomal dominant condition caused by mutation(s) in the APOB gene, encoding apolipoprotein B-100. It is characterized by hypercholesterolemia and abnormal low-density lipoproteins." @default.
- NCIT_C176014 NCIT_NHC0 "C176014" @default.
- NCIT_C176014 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C176014 NCIT_P108 "Hypercholesterolemia, Familial, 2" @default.
- NCIT_C176014 NCIT_P208 "CL1413508" @default.
- NCIT_C176014 NCIT_P322 "Cellosaurus" @default.
- NCIT_C176014 NCIT_R176 NCIT_C106030 @default.
- NCIT_C176014 NCIT_R176 NCIT_C16612 @default.
- NCIT_C176014 NCIT_R176 NCIT_C21295 @default.
- NCIT_C176014 NCIT_R176 NCIT_C28533 @default.
- NCIT_C176014 normalizedInformationContent "100" @default.
- NCIT_C176014 referenceCount "1" @default.
- NCIT_C176014 hasExactSynonym "Autosomal Dominant Hypercholesterolemia" @default.
- NCIT_C176014 hasExactSynonym "FCHL2" @default.
- NCIT_C176014 hasExactSynonym "Familial Hypercholesterolemia 2" @default.
- NCIT_C176014 hasExactSynonym "Hypercholesterolemia, Familial, 2" @default.
- NCIT_C176014 inSubset NCIT_C165258 @default.
- NCIT_C176014 inSubset NCIT_C192842 @default.
- NCIT_C176014 type Class @default.
- NCIT_C176014 isDefinedBy ncit.owl @default.
- NCIT_C176014 label "Hypercholesterolemia, Familial, 2" @default.
- NCIT_C176014 subClassOf B17fd956f52d0e8aaec060daa3f7e7482 @default.
- NCIT_C176014 subClassOf Bde251b0ebc486f6f9f69b0bd352f22a3 @default.
- NCIT_C176014 subClassOf NCIT_C176014 @default.
- NCIT_C176014 subClassOf NCIT_C2991 @default.
- NCIT_C176014 subClassOf NCIT_C3235 @default.
- NCIT_C176014 subClassOf NCIT_C34709 @default.
- NCIT_C176014 subClassOf NCIT_C53529 @default.
- NCIT_C176014 subClassOf NCIT_C53547 @default.
- NCIT_C176014 subClassOf NCIT_C7057 @default.