Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP988809.RACZJVZxhz_i936b_FRaD7cOoHM5LvPsjSNkb-EfsxgFI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP988809.RACZJVZxhz_i936b_FRaD7cOoHM5LvPsjSNkb-EfsxgFI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP988809.RACZJVZxhz_i936b_FRaD7cOoHM5LvPsjSNkb-EfsxgFI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP988809.RACZJVZxhz_i936b_FRaD7cOoHM5LvPsjSNkb-EfsxgFI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP988809.RACZJVZxhz_i936b_FRaD7cOoHM5LvPsjSNkb-EfsxgFI130_provenance.
- NP988809.RACZJVZxhz_i936b_FRaD7cOoHM5LvPsjSNkb-EfsxgFI130_assertion wasGeneratedBy ECO_0000203 NP988809.RACZJVZxhz_i936b_FRaD7cOoHM5LvPsjSNkb-EfsxgFI130_provenance.
- NP988809.RACZJVZxhz_i936b_FRaD7cOoHM5LvPsjSNkb-EfsxgFI130_assertion wasDerivedFrom befree-20150227 NP988809.RACZJVZxhz_i936b_FRaD7cOoHM5LvPsjSNkb-EfsxgFI130_provenance.
- NP988809.RACZJVZxhz_i936b_FRaD7cOoHM5LvPsjSNkb-EfsxgFI130_assertion SIO_000772 11739371 NP988809.RACZJVZxhz_i936b_FRaD7cOoHM5LvPsjSNkb-EfsxgFI130_provenance.
- NP988809.RACZJVZxhz_i936b_FRaD7cOoHM5LvPsjSNkb-EfsxgFI130_assertion evidence source_evidence_literature NP988809.RACZJVZxhz_i936b_FRaD7cOoHM5LvPsjSNkb-EfsxgFI130_provenance.
- NP988809.RACZJVZxhz_i936b_FRaD7cOoHM5LvPsjSNkb-EfsxgFI130_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." NP988809.RACZJVZxhz_i936b_FRaD7cOoHM5LvPsjSNkb-EfsxgFI130_provenance.