@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP426253.RAjIswSdkNkUMtoDYAXIauAd-eajBOXINJiNl1Yye5sxg> .
@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:NP426253.RAjIswSdkNkUMtoDYAXIauAd-eajBOXINJiNl1Yye5sxg130_head {
  this: np:hasAssertion dgn-np:NP426253.RAjIswSdkNkUMtoDYAXIauAd-eajBOXINJiNl1Yye5sxg130_assertion;
    np:hasProvenance dgn-np:NP426253.RAjIswSdkNkUMtoDYAXIauAd-eajBOXINJiNl1Yye5sxg130_provenance;
    np:hasPublicationInfo dgn-np:NP426253.RAjIswSdkNkUMtoDYAXIauAd-eajBOXINJiNl1Yye5sxg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP426253.RAjIswSdkNkUMtoDYAXIauAd-eajBOXINJiNl1Yye5sxg130_assertion a np:Assertion .
  
  dgn-np:NP426253.RAjIswSdkNkUMtoDYAXIauAd-eajBOXINJiNl1Yye5sxg130_provenance a np:Provenance .
  
  dgn-np:NP426253.RAjIswSdkNkUMtoDYAXIauAd-eajBOXINJiNl1Yye5sxg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP426253.RAjIswSdkNkUMtoDYAXIauAd-eajBOXINJiNl1Yye5sxg130_assertion {
  miriam-gene:50987 a ncit:C16612 .
  
  lld:C0751495 a ncit:C7057 .
  
  dgn-gda:DGNdd3bbfe8e443a84b50904dd1d357e950 sio:SIO_000628 miriam-gene:50987, lld:C0751495;
    a sio:SIO_001121 .
}

dgn-np:NP426253.RAjIswSdkNkUMtoDYAXIauAd-eajBOXINJiNl1Yye5sxg130_provenance {
  dgn-np:NP426253.RAjIswSdkNkUMtoDYAXIauAd-eajBOXINJiNl1Yye5sxg130_assertion dcterms:description
      "[Familial partial epilepsy with variable foci (FPEVF) is an autosomal dominant syndrome characterized by partial seizures originating from different brain regions in different family members in the absence of detectable structural abnormalities.]. 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:15329069;
    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:NP426253.RAjIswSdkNkUMtoDYAXIauAd-eajBOXINJiNl1Yye5sxg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:13+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" .
}