Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B20dede4f7c0f58af55deaaf1e52c1521> ?p ?o ?g. }
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- B20dede4f7c0f58af55deaaf1e52c1521 hasDbXref 0000-0002-0736-9199 @default.
- B20dede4f7c0f58af55deaaf1e52c1521 hasDbXref "PMID:15105360" @default.
- B20dede4f7c0f58af55deaaf1e52c1521 hasDbXref "PMID:22516080" @default.
- B20dede4f7c0f58af55deaaf1e52c1521 type Axiom @default.
- B20dede4f7c0f58af55deaaf1e52c1521 annotatedProperty IAO_0000115 @default.
- B20dede4f7c0f58af55deaaf1e52c1521 annotatedSource HP_0003642 @default.
- B20dede4f7c0f58af55deaaf1e52c1521 annotatedTarget "Abnormal transferrin isoform profile consistent with a type I congenital disorder of glycosylation. In the traditional nomenclature for congenital disorders of glycosylation, absence of entire glycans was designated type I, and loss of one or more monosaccharides as type II." @default.