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- NCIT_C85053 IAO_0000115 "The most common type of mucopolysaccharidosis. It is inherited in an autosomal recessive pattern. It comprises a group of lysosomal storage diseases which includes the most severe form (Hurler syndrome) and the mildest form (Scheie syndrome)." @default.
- NCIT_C85053 NCIT_NHC0 "C85053" @default.
- NCIT_C85053 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C85053 NCIT_P108 "Mucopolysaccharidosis Type I" @default.
- NCIT_C85053 NCIT_P207 "C0023786" @default.
- NCIT_C85053 NCIT_R176 NCIT_C115252 @default.
- NCIT_C85053 NCIT_R176 NCIT_C16612 @default.
- NCIT_C85053 NCIT_R176 NCIT_C21281 @default.
- NCIT_C85053 NCIT_R176 NCIT_C25804 @default.
- NCIT_C85053 normalizedInformationContent "88.143637090998837" @default.
- NCIT_C85053 referenceCount "6" @default.
- NCIT_C85053 hasExactSynonym "MPS I" @default.
- NCIT_C85053 hasExactSynonym "Mucopolysaccharidosis I" @default.
- NCIT_C85053 hasExactSynonym "Mucopolysaccharidosis Type I" @default.
- NCIT_C85053 type Class @default.
- NCIT_C85053 isDefinedBy ncit.owl @default.
- NCIT_C85053 label "Mucopolysaccharidosis Type I" @default.
- NCIT_C85053 subClassOf B1323a5ce47ebe3ed85fd58ca79be8be9 @default.
- NCIT_C85053 subClassOf B28ef19aba4d6f6f3c8e12ab2b734bfda @default.
- NCIT_C85053 subClassOf NCIT_C2991 @default.
- NCIT_C85053 subClassOf NCIT_C3235 @default.
- NCIT_C85053 subClassOf NCIT_C34816 @default.
- NCIT_C85053 subClassOf NCIT_C4873 @default.
- NCIT_C85053 subClassOf NCIT_C53529 @default.
- NCIT_C85053 subClassOf NCIT_C53543 @default.
- NCIT_C85053 subClassOf NCIT_C53547 @default.
- NCIT_C85053 subClassOf NCIT_C61250 @default.
- NCIT_C85053 subClassOf NCIT_C61259 @default.
- NCIT_C85053 subClassOf NCIT_C7057 @default.
- NCIT_C85053 subClassOf NCIT_C85053 @default.
- NCIT_C85053 subClassOf NCIT_C97089 @default.