Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP338556.RAVeUqbYhyecbMF9p5i7LTO6edFNKAsyIQupCmcCrmv-o130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP338556.RAVeUqbYhyecbMF9p5i7LTO6edFNKAsyIQupCmcCrmv-o130_assertion type Assertion NP338556.RAVeUqbYhyecbMF9p5i7LTO6edFNKAsyIQupCmcCrmv-o130_head.
- NP338556.RAVeUqbYhyecbMF9p5i7LTO6edFNKAsyIQupCmcCrmv-o130_assertion wasGeneratedBy ECO_0000203 NP338556.RAVeUqbYhyecbMF9p5i7LTO6edFNKAsyIQupCmcCrmv-o130_provenance.
- NP338556.RAVeUqbYhyecbMF9p5i7LTO6edFNKAsyIQupCmcCrmv-o130_assertion wasDerivedFrom befree-2016 NP338556.RAVeUqbYhyecbMF9p5i7LTO6edFNKAsyIQupCmcCrmv-o130_provenance.
- NP338556.RAVeUqbYhyecbMF9p5i7LTO6edFNKAsyIQupCmcCrmv-o130_assertion SIO_000772 11739371 NP338556.RAVeUqbYhyecbMF9p5i7LTO6edFNKAsyIQupCmcCrmv-o130_provenance.
- NP338556.RAVeUqbYhyecbMF9p5i7LTO6edFNKAsyIQupCmcCrmv-o130_assertion evidence source_evidence_literature NP338556.RAVeUqbYhyecbMF9p5i7LTO6edFNKAsyIQupCmcCrmv-o130_provenance.
- NP338556.RAVeUqbYhyecbMF9p5i7LTO6edFNKAsyIQupCmcCrmv-o130_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." NP338556.RAVeUqbYhyecbMF9p5i7LTO6edFNKAsyIQupCmcCrmv-o130_provenance.