Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP358368.RAIAcjy9srTH78cO6V6LWKe8xoRzFlNahQhTVwFbXEyDU130_assertion> ?p ?o ?g. }
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- NP358368.RAIAcjy9srTH78cO6V6LWKe8xoRzFlNahQhTVwFbXEyDU130_assertion type Assertion NP358368.RAIAcjy9srTH78cO6V6LWKe8xoRzFlNahQhTVwFbXEyDU130_head.
- NP358368.RAIAcjy9srTH78cO6V6LWKe8xoRzFlNahQhTVwFbXEyDU130_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." NP358368.RAIAcjy9srTH78cO6V6LWKe8xoRzFlNahQhTVwFbXEyDU130_provenance.
- NP358368.RAIAcjy9srTH78cO6V6LWKe8xoRzFlNahQhTVwFbXEyDU130_assertion evidence source_evidence_literature NP358368.RAIAcjy9srTH78cO6V6LWKe8xoRzFlNahQhTVwFbXEyDU130_provenance.
- NP358368.RAIAcjy9srTH78cO6V6LWKe8xoRzFlNahQhTVwFbXEyDU130_assertion SIO_000772 23404334 NP358368.RAIAcjy9srTH78cO6V6LWKe8xoRzFlNahQhTVwFbXEyDU130_provenance.
- NP358368.RAIAcjy9srTH78cO6V6LWKe8xoRzFlNahQhTVwFbXEyDU130_assertion wasDerivedFrom befree-20150227 NP358368.RAIAcjy9srTH78cO6V6LWKe8xoRzFlNahQhTVwFbXEyDU130_provenance.
- NP358368.RAIAcjy9srTH78cO6V6LWKe8xoRzFlNahQhTVwFbXEyDU130_assertion wasGeneratedBy ECO_0000203 NP358368.RAIAcjy9srTH78cO6V6LWKe8xoRzFlNahQhTVwFbXEyDU130_provenance.