Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Bff4bc49b3fcc085f087f3ad79d3b453a> ?p ?o ?g. }
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- Bff4bc49b3fcc085f087f3ad79d3b453a hasDbXref 0000-0002-0736-9199 @default.
- Bff4bc49b3fcc085f087f3ad79d3b453a hasDbXref "PMID:22516080" @default.
- Bff4bc49b3fcc085f087f3ad79d3b453a type Axiom @default.
- Bff4bc49b3fcc085f087f3ad79d3b453a annotatedProperty IAO_0000115 @default.
- Bff4bc49b3fcc085f087f3ad79d3b453a annotatedSource HP_0003160 @default.
- Bff4bc49b3fcc085f087f3ad79d3b453a annotatedTarget "Glycosylated transferrin concentrations can be measured in serum as a marker of N-linked glycosylation fidelity. 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. These terms are retained for historical reasons but for new annotations the precise glycosylation defect should be recorded." @default.