Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP222772.RACj9yxd_aIbHAhB3K364OskETJkcvLJ_6s4SeTOhhaL0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP222772.RACj9yxd_aIbHAhB3K364OskETJkcvLJ_6s4SeTOhhaL0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP222772.RACj9yxd_aIbHAhB3K364OskETJkcvLJ_6s4SeTOhhaL0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP222772.RACj9yxd_aIbHAhB3K364OskETJkcvLJ_6s4SeTOhhaL0130_provenance.
- NP222772.RACj9yxd_aIbHAhB3K364OskETJkcvLJ_6s4SeTOhhaL0130_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." NP222772.RACj9yxd_aIbHAhB3K364OskETJkcvLJ_6s4SeTOhhaL0130_provenance.
- NP222772.RACj9yxd_aIbHAhB3K364OskETJkcvLJ_6s4SeTOhhaL0130_assertion evidence source_evidence_literature NP222772.RACj9yxd_aIbHAhB3K364OskETJkcvLJ_6s4SeTOhhaL0130_provenance.
- NP222772.RACj9yxd_aIbHAhB3K364OskETJkcvLJ_6s4SeTOhhaL0130_assertion SIO_000772 23404334 NP222772.RACj9yxd_aIbHAhB3K364OskETJkcvLJ_6s4SeTOhhaL0130_provenance.
- NP222772.RACj9yxd_aIbHAhB3K364OskETJkcvLJ_6s4SeTOhhaL0130_assertion wasDerivedFrom befree-20140225 NP222772.RACj9yxd_aIbHAhB3K364OskETJkcvLJ_6s4SeTOhhaL0130_provenance.
- NP222772.RACj9yxd_aIbHAhB3K364OskETJkcvLJ_6s4SeTOhhaL0130_assertion wasGeneratedBy ECO_0000203 NP222772.RACj9yxd_aIbHAhB3K364OskETJkcvLJ_6s4SeTOhhaL0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP222772.RACj9yxd_aIbHAhB3K364OskETJkcvLJ_6s4SeTOhhaL0130_provenance.