Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B14a1c3fd1b0653a94d70e6859b18b3e7> ?p ?o ?g. }
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- B14a1c3fd1b0653a94d70e6859b18b3e7 hasDbXref "Orphanet:2363" @default.
- B14a1c3fd1b0653a94d70e6859b18b3e7 hasDbXref "https://orcid.org/0000-0001-5208-3432" @default.
- B14a1c3fd1b0653a94d70e6859b18b3e7 type Axiom @default.
- B14a1c3fd1b0653a94d70e6859b18b3e7 annotatedProperty IAO_0000115 @default.
- B14a1c3fd1b0653a94d70e6859b18b3e7 annotatedSource MONDO_0007872 @default.
- B14a1c3fd1b0653a94d70e6859b18b3e7 annotatedTarget "A multiple congenital anomaly syndrome characterized by hypoplasia, aplasia or atresia of the lacrimal system; anomalies of the ears and hearing loss; hypoplasias, apalsias or atresias of the salivary glands; dental anomalies and digital malformations." @default.