Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP988754.RA08TxyHcuaswpRUq0ervAej-VFA6uVWa74lKh1RdEpkE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP988754.RA08TxyHcuaswpRUq0ervAej-VFA6uVWa74lKh1RdEpkE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP988754.RA08TxyHcuaswpRUq0ervAej-VFA6uVWa74lKh1RdEpkE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP988754.RA08TxyHcuaswpRUq0ervAej-VFA6uVWa74lKh1RdEpkE130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP988754.RA08TxyHcuaswpRUq0ervAej-VFA6uVWa74lKh1RdEpkE130_provenance.