Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B7588413da1964c8659dfd36a8a24e2a0> ?p ?o ?g. }
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- B7588413da1964c8659dfd36a8a24e2a0 hasDbXref "Orphanet:1001" @default.
- B7588413da1964c8659dfd36a8a24e2a0 hasDbXref "https://orcid.org/0000-0001-5208-3432" @default.
- B7588413da1964c8659dfd36a8a24e2a0 type Axiom @default.
- B7588413da1964c8659dfd36a8a24e2a0 annotatedProperty IAO_0000115 @default.
- B7588413da1964c8659dfd36a8a24e2a0 annotatedSource MONDO_0010886 @default.
- B7588413da1964c8659dfd36a8a24e2a0 annotatedTarget "A chromosomal anomaly involving deletion of chromosome band 2q37 and manifests as three major clinical findings: developmental delay, skeletal malformations and facial dysmorphism." @default.