Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP428372.RAAu2DSgThYCylSb2MKjHCyZpytb0Vk6nN2b_LJEpB2iI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP428372.RAAu2DSgThYCylSb2MKjHCyZpytb0Vk6nN2b_LJEpB2iI130_assertion type Assertion NP428372.RAAu2DSgThYCylSb2MKjHCyZpytb0Vk6nN2b_LJEpB2iI130_head.
- NP428372.RAAu2DSgThYCylSb2MKjHCyZpytb0Vk6nN2b_LJEpB2iI130_assertion wasGeneratedBy ECO_0000203 NP428372.RAAu2DSgThYCylSb2MKjHCyZpytb0Vk6nN2b_LJEpB2iI130_provenance.
- NP428372.RAAu2DSgThYCylSb2MKjHCyZpytb0Vk6nN2b_LJEpB2iI130_assertion wasDerivedFrom befree-20140225 NP428372.RAAu2DSgThYCylSb2MKjHCyZpytb0Vk6nN2b_LJEpB2iI130_provenance.
- NP428372.RAAu2DSgThYCylSb2MKjHCyZpytb0Vk6nN2b_LJEpB2iI130_assertion SIO_000772 21899441 NP428372.RAAu2DSgThYCylSb2MKjHCyZpytb0Vk6nN2b_LJEpB2iI130_provenance.
- NP428372.RAAu2DSgThYCylSb2MKjHCyZpytb0Vk6nN2b_LJEpB2iI130_assertion evidence source_evidence_literature NP428372.RAAu2DSgThYCylSb2MKjHCyZpytb0Vk6nN2b_LJEpB2iI130_provenance.
- NP428372.RAAu2DSgThYCylSb2MKjHCyZpytb0Vk6nN2b_LJEpB2iI130_assertion description "[The congenital disorder of glycosylation (CDG)-Ic (ALG6-CDG, CDG-Ic) is caused by mutations in the hALG6 gene that encodes the N-glycosylation pathway enzyme, α-1,3-glucosyltransferase (NP_037471.2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP428372.RAAu2DSgThYCylSb2MKjHCyZpytb0Vk6nN2b_LJEpB2iI130_provenance.