Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP338554.RAeiJwSmNBqJ6s8NcykU83K7zcGQfNGCyciIVAr3TkGNw130_assertion> ?p ?o ?g. }
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- NP338554.RAeiJwSmNBqJ6s8NcykU83K7zcGQfNGCyciIVAr3TkGNw130_assertion type Assertion NP338554.RAeiJwSmNBqJ6s8NcykU83K7zcGQfNGCyciIVAr3TkGNw130_head.
- NP338554.RAeiJwSmNBqJ6s8NcykU83K7zcGQfNGCyciIVAr3TkGNw130_assertion wasGeneratedBy ECO_0000203 NP338554.RAeiJwSmNBqJ6s8NcykU83K7zcGQfNGCyciIVAr3TkGNw130_provenance.
- NP338554.RAeiJwSmNBqJ6s8NcykU83K7zcGQfNGCyciIVAr3TkGNw130_assertion wasDerivedFrom befree-2016 NP338554.RAeiJwSmNBqJ6s8NcykU83K7zcGQfNGCyciIVAr3TkGNw130_provenance.
- NP338554.RAeiJwSmNBqJ6s8NcykU83K7zcGQfNGCyciIVAr3TkGNw130_assertion SIO_000772 11739371 NP338554.RAeiJwSmNBqJ6s8NcykU83K7zcGQfNGCyciIVAr3TkGNw130_provenance.
- NP338554.RAeiJwSmNBqJ6s8NcykU83K7zcGQfNGCyciIVAr3TkGNw130_assertion evidence source_evidence_literature NP338554.RAeiJwSmNBqJ6s8NcykU83K7zcGQfNGCyciIVAr3TkGNw130_provenance.
- NP338554.RAeiJwSmNBqJ6s8NcykU83K7zcGQfNGCyciIVAr3TkGNw130_assertion description "[Lafora disease (progressive myoclonus epilepsy of Lafora type) is an autosomal recessive neurodegenerative disorder resulting from defects in the EPM2A gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP338554.RAeiJwSmNBqJ6s8NcykU83K7zcGQfNGCyciIVAr3TkGNw130_provenance.