@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP597115.RAld3rXiWkG-Qd1apJz7lKj7-TzowBTV8wzI3CdXcvusU> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP597115.RAld3rXiWkG-Qd1apJz7lKj7-TzowBTV8wzI3CdXcvusU130_head {
  this: np:hasAssertion dgn-np:NP597115.RAld3rXiWkG-Qd1apJz7lKj7-TzowBTV8wzI3CdXcvusU130_assertion;
    np:hasProvenance dgn-np:NP597115.RAld3rXiWkG-Qd1apJz7lKj7-TzowBTV8wzI3CdXcvusU130_provenance;
    np:hasPublicationInfo dgn-np:NP597115.RAld3rXiWkG-Qd1apJz7lKj7-TzowBTV8wzI3CdXcvusU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP597115.RAld3rXiWkG-Qd1apJz7lKj7-TzowBTV8wzI3CdXcvusU130_assertion a np:Assertion .
  
  dgn-np:NP597115.RAld3rXiWkG-Qd1apJz7lKj7-TzowBTV8wzI3CdXcvusU130_provenance a np:Provenance .
  
  dgn-np:NP597115.RAld3rXiWkG-Qd1apJz7lKj7-TzowBTV8wzI3CdXcvusU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP597115.RAld3rXiWkG-Qd1apJz7lKj7-TzowBTV8wzI3CdXcvusU130_assertion {
  miriam-gene:114327 a ncit:C16612 .
  
  lld:C0270853 a ncit:C7057 .
  
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dgn-np:NP597115.RAld3rXiWkG-Qd1apJz7lKj7-TzowBTV8wzI3CdXcvusU130_provenance {
  dgn-np:NP597115.RAld3rXiWkG-Qd1apJz7lKj7-TzowBTV8wzI3CdXcvusU130_assertion dcterms:description
      "[In the second part of this chapter, we will also propose a new point of view on how some structural genes could, under certain conditions, when altered, produced idiopathic generalized epilepsy with myoclonic jerks, taking juvenile myoclonic epilepsy (JME) and the myoclonin (EFHC-1) gene as examples.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
    sio:SIO_000772 miriam-pubmed:17336771;
    prov:wasDerivedFrom dgn-void:befree-2016;
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  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^xsd:date .
  
  dgn-void:source_evidence_literature a eco:ECO_0000212;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}

dgn-np:NP597115.RAld3rXiWkG-Qd1apJz7lKj7-TzowBTV8wzI3CdXcvusU130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:16+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
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    pav:authoredBy <http://orcid.org/0000-0001-5999-6269>, <http://orcid.org/0000-0002-7534-7661>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
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  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}