Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP988754.RA08TxyHcuaswpRUq0ervAej-VFA6uVWa74lKh1RdEpkE130_assertion> ?p ?o ?g. }
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- NP988754.RA08TxyHcuaswpRUq0ervAej-VFA6uVWa74lKh1RdEpkE130_assertion type Assertion NP988754.RA08TxyHcuaswpRUq0ervAej-VFA6uVWa74lKh1RdEpkE130_head.
- NP988754.RA08TxyHcuaswpRUq0ervAej-VFA6uVWa74lKh1RdEpkE130_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." NP988754.RA08TxyHcuaswpRUq0ervAej-VFA6uVWa74lKh1RdEpkE130_provenance.
- NP988754.RA08TxyHcuaswpRUq0ervAej-VFA6uVWa74lKh1RdEpkE130_assertion evidence source_evidence_literature NP988754.RA08TxyHcuaswpRUq0ervAej-VFA6uVWa74lKh1RdEpkE130_provenance.
- NP988754.RA08TxyHcuaswpRUq0ervAej-VFA6uVWa74lKh1RdEpkE130_assertion SIO_000772 23278576 NP988754.RA08TxyHcuaswpRUq0ervAej-VFA6uVWa74lKh1RdEpkE130_provenance.
- NP988754.RA08TxyHcuaswpRUq0ervAej-VFA6uVWa74lKh1RdEpkE130_assertion wasDerivedFrom befree-20150227 NP988754.RA08TxyHcuaswpRUq0ervAej-VFA6uVWa74lKh1RdEpkE130_provenance.
- NP988754.RA08TxyHcuaswpRUq0ervAej-VFA6uVWa74lKh1RdEpkE130_assertion wasGeneratedBy ECO_0000203 NP988754.RA08TxyHcuaswpRUq0ervAej-VFA6uVWa74lKh1RdEpkE130_provenance.