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- NP455148.RAo6-MoV0v_crRFwOjI_YUJcumKeFbhjzbmF6NG-6e5m0130_assertion type Assertion NP455148.RAo6-MoV0v_crRFwOjI_YUJcumKeFbhjzbmF6NG-6e5m0130_head.
- NP455148.RAo6-MoV0v_crRFwOjI_YUJcumKeFbhjzbmF6NG-6e5m0130_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." NP455148.RAo6-MoV0v_crRFwOjI_YUJcumKeFbhjzbmF6NG-6e5m0130_provenance.
- NP455148.RAo6-MoV0v_crRFwOjI_YUJcumKeFbhjzbmF6NG-6e5m0130_assertion evidence source_evidence_literature NP455148.RAo6-MoV0v_crRFwOjI_YUJcumKeFbhjzbmF6NG-6e5m0130_provenance.
- NP455148.RAo6-MoV0v_crRFwOjI_YUJcumKeFbhjzbmF6NG-6e5m0130_assertion SIO_000772 23278576 NP455148.RAo6-MoV0v_crRFwOjI_YUJcumKeFbhjzbmF6NG-6e5m0130_provenance.
- NP455148.RAo6-MoV0v_crRFwOjI_YUJcumKeFbhjzbmF6NG-6e5m0130_assertion wasDerivedFrom befree-20140225 NP455148.RAo6-MoV0v_crRFwOjI_YUJcumKeFbhjzbmF6NG-6e5m0130_provenance.
- NP455148.RAo6-MoV0v_crRFwOjI_YUJcumKeFbhjzbmF6NG-6e5m0130_assertion wasGeneratedBy ECO_0000203 NP455148.RAo6-MoV0v_crRFwOjI_YUJcumKeFbhjzbmF6NG-6e5m0130_provenance.