Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP715703.RAZmv2edvF4Gdp19xPIUGfZ-HxH2W8ZXSijUcv1I65dw4130_assertion> ?p ?o ?g. }
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- NP715703.RAZmv2edvF4Gdp19xPIUGfZ-HxH2W8ZXSijUcv1I65dw4130_assertion type Assertion NP715703.RAZmv2edvF4Gdp19xPIUGfZ-HxH2W8ZXSijUcv1I65dw4130_head.
- NP715703.RAZmv2edvF4Gdp19xPIUGfZ-HxH2W8ZXSijUcv1I65dw4130_assertion description "[Congenital disorders of glycosylation (CDG) comprise a rapidly growing group of inherited disorders in which glycosylation of glycoproteins is defective due to mutations in genes required for the assembly of lipid-linked oligosaccharides, their transfer to nascent glycoproteins (CDG-I) or the processing of protein-bound glycans (CDG-II).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP715703.RAZmv2edvF4Gdp19xPIUGfZ-HxH2W8ZXSijUcv1I65dw4130_provenance.
- NP715703.RAZmv2edvF4Gdp19xPIUGfZ-HxH2W8ZXSijUcv1I65dw4130_assertion evidence source_evidence_literature NP715703.RAZmv2edvF4Gdp19xPIUGfZ-HxH2W8ZXSijUcv1I65dw4130_provenance.
- NP715703.RAZmv2edvF4Gdp19xPIUGfZ-HxH2W8ZXSijUcv1I65dw4130_assertion SIO_000772 11326280 NP715703.RAZmv2edvF4Gdp19xPIUGfZ-HxH2W8ZXSijUcv1I65dw4130_provenance.
- NP715703.RAZmv2edvF4Gdp19xPIUGfZ-HxH2W8ZXSijUcv1I65dw4130_assertion wasDerivedFrom befree-20140225 NP715703.RAZmv2edvF4Gdp19xPIUGfZ-HxH2W8ZXSijUcv1I65dw4130_provenance.
- NP715703.RAZmv2edvF4Gdp19xPIUGfZ-HxH2W8ZXSijUcv1I65dw4130_assertion wasGeneratedBy ECO_0000203 NP715703.RAZmv2edvF4Gdp19xPIUGfZ-HxH2W8ZXSijUcv1I65dw4130_provenance.