@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP621413.RAInEXcfwhhlk5CkE09IO4G0_KbB3LaGLAayGbGd6o_8s> .
@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/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@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/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .

dgn-np:NP621413.RAInEXcfwhhlk5CkE09IO4G0_KbB3LaGLAayGbGd6o_8s130_head {
  this: np:hasAssertion dgn-np:NP621413.RAInEXcfwhhlk5CkE09IO4G0_KbB3LaGLAayGbGd6o_8s130_assertion;
    np:hasProvenance dgn-np:NP621413.RAInEXcfwhhlk5CkE09IO4G0_KbB3LaGLAayGbGd6o_8s130_provenance;
    np:hasPublicationInfo dgn-np:NP621413.RAInEXcfwhhlk5CkE09IO4G0_KbB3LaGLAayGbGd6o_8s130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP621413.RAInEXcfwhhlk5CkE09IO4G0_KbB3LaGLAayGbGd6o_8s130_assertion a np:Assertion .
  
  dgn-np:NP621413.RAInEXcfwhhlk5CkE09IO4G0_KbB3LaGLAayGbGd6o_8s130_provenance a np:Provenance .
  
  dgn-np:NP621413.RAInEXcfwhhlk5CkE09IO4G0_KbB3LaGLAayGbGd6o_8s130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP621413.RAInEXcfwhhlk5CkE09IO4G0_KbB3LaGLAayGbGd6o_8s130_assertion {
  miriam-gene:761 a ncit:C16612 .
  
  lld:C0009952 a ncit:C7057 .
  
  dgn-gda:DGN23902e10a5125bfe2ea91130e5cf1a71 sio:SIO_000628 miriam-gene:761, lld:C0009952;
    a sio:SIO_001121 .
}

dgn-np:NP621413.RAInEXcfwhhlk5CkE09IO4G0_KbB3LaGLAayGbGd6o_8s130_provenance {
  dgn-np:NP621413.RAInEXcfwhhlk5CkE09IO4G0_KbB3LaGLAayGbGd6o_8s130_assertion dcterms:description
      "[In order to investigate IPI influence on the transcriptional phenotype underlying RMTLE we comparatively analyzed the transcriptomic signatures of CA3 explants surgically obtained from RMTLE patients with (FS) or without (NFS) febrile seizure history.]. 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:22022585;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP621413.RAInEXcfwhhlk5CkE09IO4G0_KbB3LaGLAayGbGd6o_8s130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:15+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
    dcterms:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269>, <http://orcid.org/0000-0002-7534-7661>,
      <http://orcid.org/0000-0002-9383-528X>, <http://orcid.org/0000-0003-0169-8159>, <http://orcid.org/0000-0003-1244-7654>;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}