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- NCIT_C187989 IAO_0000115 "An X-linked condition caused by mutation(s) in the BGN gene, encoding biglycan. It is characterized by cardiovascular defects and abnormal facies." @default.
- NCIT_C187989 NCIT_NHC0 "C187989" @default.
- NCIT_C187989 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C187989 NCIT_P108 "Meester-Loeys Syndrome" @default.
- NCIT_C187989 NCIT_P208 "CL602434" @default.
- NCIT_C187989 NCIT_P322 "Cellosaurus" @default.
- NCIT_C187989 NCIT_R176 NCIT_C105838 @default.
- NCIT_C187989 NCIT_R176 NCIT_C16612 @default.
- NCIT_C187989 NCIT_R176 NCIT_C20744 @default.
- NCIT_C187989 NCIT_R176 NCIT_C26000 @default.
- NCIT_C187989 normalizedInformationContent "100" @default.
- NCIT_C187989 referenceCount "1" @default.
- NCIT_C187989 hasExactSynonym "MRLS" @default.
- NCIT_C187989 hasExactSynonym "Meester-Loeys Syndrome" @default.
- NCIT_C187989 inSubset NCIT_C165258 @default.
- NCIT_C187989 inSubset NCIT_C192842 @default.
- NCIT_C187989 type Class @default.
- NCIT_C187989 isDefinedBy ncit.owl @default.
- NCIT_C187989 label "Meester-Loeys Syndrome" @default.
- NCIT_C187989 subClassOf B9a9332b93033cc7a72d107a82b4510a7 @default.
- NCIT_C187989 subClassOf Bccb71064cff3ece3fc3a6232b5c1c106 @default.
- NCIT_C187989 subClassOf NCIT_C187989 @default.
- NCIT_C187989 subClassOf NCIT_C28193 @default.
- NCIT_C187989 subClassOf NCIT_C2991 @default.
- NCIT_C187989 subClassOf NCIT_C7057 @default.