Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Bc20ce0197956e57adb0926f4cc075c03> ?p ?o ?g. }
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- Bc20ce0197956e57adb0926f4cc075c03 hasDbXref "http://dx.doi.org/10.1155/2015/781294" @default.
- Bc20ce0197956e57adb0926f4cc075c03 type Axiom @default.
- Bc20ce0197956e57adb0926f4cc075c03 annotatedProperty IAO_0000115 @default.
- Bc20ce0197956e57adb0926f4cc075c03 annotatedSource MONDO_0020216 @default.
- Bc20ce0197956e57adb0926f4cc075c03 annotatedTarget "A hereditary disease that is associated with congenital ocular anomalies such as conditions associated with mesodermal dysgenesis of the neural crest, phakomatoses characterized by hamartomas, metabolic disorders, mitotic disorders, and other congenital disorders and associated with acquired conditions such as tumors, uveitis, and trauma." @default.