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Matches in Ubergraph for { <http://purl.obolibrary.org/obo/NCIT_C179930> ?p ?o ?g. }

• NCIT_C179930 IAO_0000115 "An autosomal dominant condition caused by mutation(s) in the PTEN gene, encoding phosphatidylinositol 3,4,5-trisphosphate 3-phosphatase and dual-specificity protein phosphatase PTEN. It is considered a type of PTEN-hamartoma syndrome. It has many features in common with Proteus syndrome, including hamartomous overgrowth of multiple tissues, cerebriform connective tissue nevi, vascular malformations and linear epidermal nevi, but has not been associated with AKT1 gene mutation(s)." @default.
• NCIT_C179930 NCIT_NHC0 "C179930" @default.
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• NCIT_C179930 NCIT_P108 "Proteus-Like Syndrome" @default.
• NCIT_C179930 NCIT_P207 "C1866398" @default.
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• NCIT_C179930 normalizedInformationContent "100" @default.
• NCIT_C179930 referenceCount "1" @default.
• NCIT_C179930 hasExactSynonym "Proteus-Like Syndrome" @default.

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