Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP338555.RA7VZ9k9OBQJ6dJbQlcX9viF28kRQ8VPdpwFwHdzhXG48130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP338555.RA7VZ9k9OBQJ6dJbQlcX9viF28kRQ8VPdpwFwHdzhXG48130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP338555.RA7VZ9k9OBQJ6dJbQlcX9viF28kRQ8VPdpwFwHdzhXG48130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP338555.RA7VZ9k9OBQJ6dJbQlcX9viF28kRQ8VPdpwFwHdzhXG48130_provenance.
- befree-2016 importedOn "2016-02-19" NP338555.RA7VZ9k9OBQJ6dJbQlcX9viF28kRQ8VPdpwFwHdzhXG48130_provenance.
- NP338555.RA7VZ9k9OBQJ6dJbQlcX9viF28kRQ8VPdpwFwHdzhXG48130_assertion wasGeneratedBy ECO_0000203 NP338555.RA7VZ9k9OBQJ6dJbQlcX9viF28kRQ8VPdpwFwHdzhXG48130_provenance.
- NP338555.RA7VZ9k9OBQJ6dJbQlcX9viF28kRQ8VPdpwFwHdzhXG48130_assertion wasDerivedFrom befree-2016 NP338555.RA7VZ9k9OBQJ6dJbQlcX9viF28kRQ8VPdpwFwHdzhXG48130_provenance.
- NP338555.RA7VZ9k9OBQJ6dJbQlcX9viF28kRQ8VPdpwFwHdzhXG48130_assertion SIO_000772 11739371 NP338555.RA7VZ9k9OBQJ6dJbQlcX9viF28kRQ8VPdpwFwHdzhXG48130_provenance.
- NP338555.RA7VZ9k9OBQJ6dJbQlcX9viF28kRQ8VPdpwFwHdzhXG48130_assertion evidence source_evidence_literature NP338555.RA7VZ9k9OBQJ6dJbQlcX9viF28kRQ8VPdpwFwHdzhXG48130_provenance.
- NP338555.RA7VZ9k9OBQJ6dJbQlcX9viF28kRQ8VPdpwFwHdzhXG48130_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." NP338555.RA7VZ9k9OBQJ6dJbQlcX9viF28kRQ8VPdpwFwHdzhXG48130_provenance.