Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP855643.RAwv4iqdrp2R_WbHELqqSGFBb6-6yqGPFxXQXNiLTG4wA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP855643.RAwv4iqdrp2R_WbHELqqSGFBb6-6yqGPFxXQXNiLTG4wA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP855643.RAwv4iqdrp2R_WbHELqqSGFBb6-6yqGPFxXQXNiLTG4wA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP855643.RAwv4iqdrp2R_WbHELqqSGFBb6-6yqGPFxXQXNiLTG4wA130_provenance.
- NP855643.RAwv4iqdrp2R_WbHELqqSGFBb6-6yqGPFxXQXNiLTG4wA130_assertion description "[Seizure disorder was common (43%) in our cohort of patients with a GLUD1 mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP855643.RAwv4iqdrp2R_WbHELqqSGFBb6-6yqGPFxXQXNiLTG4wA130_provenance.
- NP855643.RAwv4iqdrp2R_WbHELqqSGFBb6-6yqGPFxXQXNiLTG4wA130_assertion evidence source_evidence_literature NP855643.RAwv4iqdrp2R_WbHELqqSGFBb6-6yqGPFxXQXNiLTG4wA130_provenance.
- NP855643.RAwv4iqdrp2R_WbHELqqSGFBb6-6yqGPFxXQXNiLTG4wA130_assertion SIO_000772 19690084 NP855643.RAwv4iqdrp2R_WbHELqqSGFBb6-6yqGPFxXQXNiLTG4wA130_provenance.
- NP855643.RAwv4iqdrp2R_WbHELqqSGFBb6-6yqGPFxXQXNiLTG4wA130_assertion wasDerivedFrom befree-20140225 NP855643.RAwv4iqdrp2R_WbHELqqSGFBb6-6yqGPFxXQXNiLTG4wA130_provenance.
- NP855643.RAwv4iqdrp2R_WbHELqqSGFBb6-6yqGPFxXQXNiLTG4wA130_assertion wasGeneratedBy ECO_0000203 NP855643.RAwv4iqdrp2R_WbHELqqSGFBb6-6yqGPFxXQXNiLTG4wA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP855643.RAwv4iqdrp2R_WbHELqqSGFBb6-6yqGPFxXQXNiLTG4wA130_provenance.