Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP537184.RAtG4nebKEKD9zn46NBGxg9KPFG-8R-Xn_lRh2ibGRt44130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP537184.RAtG4nebKEKD9zn46NBGxg9KPFG-8R-Xn_lRh2ibGRt44130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP537184.RAtG4nebKEKD9zn46NBGxg9KPFG-8R-Xn_lRh2ibGRt44130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP537184.RAtG4nebKEKD9zn46NBGxg9KPFG-8R-Xn_lRh2ibGRt44130_provenance.
- NP537184.RAtG4nebKEKD9zn46NBGxg9KPFG-8R-Xn_lRh2ibGRt44130_assertion description "[Identification of DPAGT1, ALG14 and ALG2 mutations as a cause of congenital myasthenic syndrome underscores the importance of asparagine-linked protein glycosylation for proper functioning of the neuromuscular junction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP537184.RAtG4nebKEKD9zn46NBGxg9KPFG-8R-Xn_lRh2ibGRt44130_provenance.
- NP537184.RAtG4nebKEKD9zn46NBGxg9KPFG-8R-Xn_lRh2ibGRt44130_assertion evidence source_evidence_literature NP537184.RAtG4nebKEKD9zn46NBGxg9KPFG-8R-Xn_lRh2ibGRt44130_provenance.
- NP537184.RAtG4nebKEKD9zn46NBGxg9KPFG-8R-Xn_lRh2ibGRt44130_assertion SIO_000772 23404334 NP537184.RAtG4nebKEKD9zn46NBGxg9KPFG-8R-Xn_lRh2ibGRt44130_provenance.
- NP537184.RAtG4nebKEKD9zn46NBGxg9KPFG-8R-Xn_lRh2ibGRt44130_assertion wasDerivedFrom befree-20140225 NP537184.RAtG4nebKEKD9zn46NBGxg9KPFG-8R-Xn_lRh2ibGRt44130_provenance.
- NP537184.RAtG4nebKEKD9zn46NBGxg9KPFG-8R-Xn_lRh2ibGRt44130_assertion wasGeneratedBy ECO_0000203 NP537184.RAtG4nebKEKD9zn46NBGxg9KPFG-8R-Xn_lRh2ibGRt44130_provenance.
- befree-20140225 importedOn "2014-02-25" NP537184.RAtG4nebKEKD9zn46NBGxg9KPFG-8R-Xn_lRh2ibGRt44130_provenance.