Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1316622.RAhc5ooJGCajhFU8FuG1YAkfe0aALx5S7ATl4mmCI9gVA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1316622.RAhc5ooJGCajhFU8FuG1YAkfe0aALx5S7ATl4mmCI9gVA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1316622.RAhc5ooJGCajhFU8FuG1YAkfe0aALx5S7ATl4mmCI9gVA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1316622.RAhc5ooJGCajhFU8FuG1YAkfe0aALx5S7ATl4mmCI9gVA130_provenance.
- NP1316622.RAhc5ooJGCajhFU8FuG1YAkfe0aALx5S7ATl4mmCI9gVA130_assertion description "[Our results demonstrate that (1) the genetic susceptibility to idiopathic absence epilepsies and broader spectra of IGEs is heterogeneous, (2) the gene effect of EJM1 depends on the familial genetic background, and (3) EJM1 confers genetic susceptibility to idiopathic absence epilepsies and broader spectra of IGEs in the presence of family members with JME.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1316622.RAhc5ooJGCajhFU8FuG1YAkfe0aALx5S7ATl4mmCI9gVA130_provenance.
- NP1316622.RAhc5ooJGCajhFU8FuG1YAkfe0aALx5S7ATl4mmCI9gVA130_assertion evidence source_evidence_literature NP1316622.RAhc5ooJGCajhFU8FuG1YAkfe0aALx5S7ATl4mmCI9gVA130_provenance.
- NP1316622.RAhc5ooJGCajhFU8FuG1YAkfe0aALx5S7ATl4mmCI9gVA130_assertion SIO_000772 7654068 NP1316622.RAhc5ooJGCajhFU8FuG1YAkfe0aALx5S7ATl4mmCI9gVA130_provenance.
- NP1316622.RAhc5ooJGCajhFU8FuG1YAkfe0aALx5S7ATl4mmCI9gVA130_assertion wasDerivedFrom befree-2016 NP1316622.RAhc5ooJGCajhFU8FuG1YAkfe0aALx5S7ATl4mmCI9gVA130_provenance.
- NP1316622.RAhc5ooJGCajhFU8FuG1YAkfe0aALx5S7ATl4mmCI9gVA130_assertion wasGeneratedBy ECO_0000203 NP1316622.RAhc5ooJGCajhFU8FuG1YAkfe0aALx5S7ATl4mmCI9gVA130_provenance.
- befree-2016 importedOn "2016-02-19" NP1316622.RAhc5ooJGCajhFU8FuG1YAkfe0aALx5S7ATl4mmCI9gVA130_provenance.