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Matches in Ubergraph for { <http://purl.obolibrary.org/obo/NCIT_C176943> ?p ?o ?g. }

• NCIT_C176943 IAO_0000115 "A rare inherited form of myofibromatosis caused by autosomal dominant mutation(s) in the PDGFRB gene, encoding platelet-derived growth factor receptor beta. The condition is characterized by the onset of solitary or multicentric benign tumors in the skin, striated muscles, bones, and viscera. The lesions may be present at birth or become apparent in early infancy or even occasionally in adult life." @default.
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• NCIT_C176943 NCIT_P108 "Infantile Myofibromatosis 1" @default.
• NCIT_C176943 NCIT_P207 "C0432284" @default.
• NCIT_C176943 NCIT_P363 "Benign" @default.
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• NCIT_C176943 normalizedInformationContent "92.730304365937428" @default.
• NCIT_C176943 referenceCount "3" @default.
• NCIT_C176943 hasExactSynonym "IMF1" @default.
• NCIT_C176943 hasExactSynonym "Infantile Myofibromatosis 1" @default.
• NCIT_C176943 type Class @default.
• NCIT_C176943 isDefinedBy ncit.owl @default.
• NCIT_C176943 label "Infantile Myofibromatosis 1" @default.
• NCIT_C176943 subClassOf NCIT_C176943 @default.
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• NCIT_C176943 subClassOf NCIT_C3677 @default.
• NCIT_C176943 subClassOf NCIT_C3742 @default.

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