Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP307085.RAW9gPhmym8vJFQOaXDPU5sJ_ZkCtWPOlYgeS6lfeqm38130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP307085.RAW9gPhmym8vJFQOaXDPU5sJ_ZkCtWPOlYgeS6lfeqm38130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP307085.RAW9gPhmym8vJFQOaXDPU5sJ_ZkCtWPOlYgeS6lfeqm38130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP307085.RAW9gPhmym8vJFQOaXDPU5sJ_ZkCtWPOlYgeS6lfeqm38130_provenance.
- NP307085.RAW9gPhmym8vJFQOaXDPU5sJ_ZkCtWPOlYgeS6lfeqm38130_assertion description "[Mutational spectrum of the EPM2A gene in progressive myoclonus epilepsy of Lafora: high degree of allelic heterogeneity and prevalence of deletions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP307085.RAW9gPhmym8vJFQOaXDPU5sJ_ZkCtWPOlYgeS6lfeqm38130_provenance.
- NP307085.RAW9gPhmym8vJFQOaXDPU5sJ_ZkCtWPOlYgeS6lfeqm38130_assertion evidence source_evidence_literature NP307085.RAW9gPhmym8vJFQOaXDPU5sJ_ZkCtWPOlYgeS6lfeqm38130_provenance.
- NP307085.RAW9gPhmym8vJFQOaXDPU5sJ_ZkCtWPOlYgeS6lfeqm38130_assertion SIO_000772 11175283 NP307085.RAW9gPhmym8vJFQOaXDPU5sJ_ZkCtWPOlYgeS6lfeqm38130_provenance.
- NP307085.RAW9gPhmym8vJFQOaXDPU5sJ_ZkCtWPOlYgeS6lfeqm38130_assertion wasDerivedFrom befree-2016 NP307085.RAW9gPhmym8vJFQOaXDPU5sJ_ZkCtWPOlYgeS6lfeqm38130_provenance.
- NP307085.RAW9gPhmym8vJFQOaXDPU5sJ_ZkCtWPOlYgeS6lfeqm38130_assertion wasGeneratedBy ECO_0000203 NP307085.RAW9gPhmym8vJFQOaXDPU5sJ_ZkCtWPOlYgeS6lfeqm38130_provenance.
- befree-2016 importedOn "2016-02-19" NP307085.RAW9gPhmym8vJFQOaXDPU5sJ_ZkCtWPOlYgeS6lfeqm38130_provenance.