Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B60a54e1fc62857fb74b05b0cf7f7b8c6> ?p ?o ?g. }
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- B60a54e1fc62857fb74b05b0cf7f7b8c6 hasDbXref "Orphanet:3378" @default.
- B60a54e1fc62857fb74b05b0cf7f7b8c6 type Axiom @default.
- B60a54e1fc62857fb74b05b0cf7f7b8c6 annotatedProperty IAO_0000115 @default.
- B60a54e1fc62857fb74b05b0cf7f7b8c6 annotatedSource MONDO_0018068 @default.
- B60a54e1fc62857fb74b05b0cf7f7b8c6 annotatedTarget "Trisomy 13 is a chromosomal anomaly caused by the presence of an extra chromosome 13 and is characterized by brain malformations (holoprosencephaly), facial dysmorphism, ocular anomalies, postaxial polydactyly, visceral malformations (cardiopathy) and severe psychomotor retardation." @default.