Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1117072.RAdlCooMpGRIIiy3toVmk3xK500NJkLUXn1A4X3EQGGJg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1117072.RAdlCooMpGRIIiy3toVmk3xK500NJkLUXn1A4X3EQGGJg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1117072.RAdlCooMpGRIIiy3toVmk3xK500NJkLUXn1A4X3EQGGJg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1117072.RAdlCooMpGRIIiy3toVmk3xK500NJkLUXn1A4X3EQGGJg130_provenance.
- NP1117072.RAdlCooMpGRIIiy3toVmk3xK500NJkLUXn1A4X3EQGGJg130_assertion description "[PRRT2 mutations do not seem to be involved in the aetiology of FS or infantile epileptic encephalopathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1117072.RAdlCooMpGRIIiy3toVmk3xK500NJkLUXn1A4X3EQGGJg130_provenance.
- NP1117072.RAdlCooMpGRIIiy3toVmk3xK500NJkLUXn1A4X3EQGGJg130_assertion evidence source_evidence_literature NP1117072.RAdlCooMpGRIIiy3toVmk3xK500NJkLUXn1A4X3EQGGJg130_provenance.
- NP1117072.RAdlCooMpGRIIiy3toVmk3xK500NJkLUXn1A4X3EQGGJg130_assertion SIO_000772 24101679 NP1117072.RAdlCooMpGRIIiy3toVmk3xK500NJkLUXn1A4X3EQGGJg130_provenance.
- NP1117072.RAdlCooMpGRIIiy3toVmk3xK500NJkLUXn1A4X3EQGGJg130_assertion wasDerivedFrom befree-2016 NP1117072.RAdlCooMpGRIIiy3toVmk3xK500NJkLUXn1A4X3EQGGJg130_provenance.
- NP1117072.RAdlCooMpGRIIiy3toVmk3xK500NJkLUXn1A4X3EQGGJg130_assertion wasGeneratedBy ECO_0000203 NP1117072.RAdlCooMpGRIIiy3toVmk3xK500NJkLUXn1A4X3EQGGJg130_provenance.
- befree-2016 importedOn "2016-02-19" NP1117072.RAdlCooMpGRIIiy3toVmk3xK500NJkLUXn1A4X3EQGGJg130_provenance.