Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP762779.RAzWi815r5QzeJa2uN8GCY_Un5BduIuO2txOg9J3M4MOw130_assertion> ?p ?o ?g. }
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- NP762779.RAzWi815r5QzeJa2uN8GCY_Un5BduIuO2txOg9J3M4MOw130_assertion type Assertion NP762779.RAzWi815r5QzeJa2uN8GCY_Un5BduIuO2txOg9J3M4MOw130_head.
- NP762779.RAzWi815r5QzeJa2uN8GCY_Un5BduIuO2txOg9J3M4MOw130_assertion description "[Human mutations in COLQ, LAMB2, and AGRN cause congenital myasthenic syndromes (CMSs) owing to deficiency of ColQ, laminin-?2, and agrin, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP762779.RAzWi815r5QzeJa2uN8GCY_Un5BduIuO2txOg9J3M4MOw130_provenance.
- NP762779.RAzWi815r5QzeJa2uN8GCY_Un5BduIuO2txOg9J3M4MOw130_assertion evidence source_evidence_literature NP762779.RAzWi815r5QzeJa2uN8GCY_Un5BduIuO2txOg9J3M4MOw130_provenance.
- NP762779.RAzWi815r5QzeJa2uN8GCY_Un5BduIuO2txOg9J3M4MOw130_assertion SIO_000772 23278576 NP762779.RAzWi815r5QzeJa2uN8GCY_Un5BduIuO2txOg9J3M4MOw130_provenance.
- NP762779.RAzWi815r5QzeJa2uN8GCY_Un5BduIuO2txOg9J3M4MOw130_assertion wasDerivedFrom befree-20140225 NP762779.RAzWi815r5QzeJa2uN8GCY_Un5BduIuO2txOg9J3M4MOw130_provenance.
- NP762779.RAzWi815r5QzeJa2uN8GCY_Un5BduIuO2txOg9J3M4MOw130_assertion wasGeneratedBy ECO_0000203 NP762779.RAzWi815r5QzeJa2uN8GCY_Un5BduIuO2txOg9J3M4MOw130_provenance.