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- NCIT_C130994 IAO_0000115 "Growth hormone insensitivity syndrome caused by mutation(s) and/or deletion(s) in the GHR gene, encoding the growth hormone receptor." @default.
- NCIT_C130994 NCIT_NHC0 "C130994" @default.
- NCIT_C130994 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C130994 NCIT_P108 "Laron Syndrome" @default.
- NCIT_C130994 NCIT_P208 "CL513965" @default.
- NCIT_C130994 NCIT_P322 "NICHD" @default.
- NCIT_C130994 NCIT_P325 "Growth hormone insensitivity syndrome caused by mutation(s) and/or deletion(s) in the GHR gene, encoding the growth hormone receptor." @default.
- NCIT_C130994 NCIT_R176 NCIT_C16612 @default.
- NCIT_C130994 NCIT_R176 NCIT_C20103 @default.
- NCIT_C130994 NCIT_R176 NCIT_C21295 @default.
- NCIT_C130994 NCIT_R176 NCIT_C41016 @default.
- NCIT_C130994 normalizedInformationContent "100" @default.
- NCIT_C130994 referenceCount "1" @default.
- NCIT_C130994 hasExactSynonym "Growth Hormone Receptor Deficiency" @default.
- NCIT_C130994 hasExactSynonym "Laron Syndrome" @default.
- NCIT_C130994 inSubset NCIT_C118467 @default.
- NCIT_C130994 inSubset NCIT_C90259 @default.
- NCIT_C130994 type Class @default.
- NCIT_C130994 isDefinedBy ncit.owl @default.
- NCIT_C130994 label "Laron Syndrome" @default.
- NCIT_C130994 subClassOf Bae7af26db5c2649795d05eec8da111e4 @default.
- NCIT_C130994 subClassOf Bc35d2337114cc29c31975ecb58165be7 @default.
- NCIT_C130994 subClassOf NCIT_C130994 @default.
- NCIT_C130994 subClassOf NCIT_C28193 @default.
- NCIT_C130994 subClassOf NCIT_C2991 @default.
- NCIT_C130994 subClassOf NCIT_C7057 @default.