@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP787668.RAnU1GgnyyQccRb7wqae6XZr7WOilKcQn2LuI1htIVNXU> .
@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:NP787668.RAnU1GgnyyQccRb7wqae6XZr7WOilKcQn2LuI1htIVNXU130_head {
  this: np:hasAssertion dgn-np:NP787668.RAnU1GgnyyQccRb7wqae6XZr7WOilKcQn2LuI1htIVNXU130_assertion;
    np:hasProvenance dgn-np:NP787668.RAnU1GgnyyQccRb7wqae6XZr7WOilKcQn2LuI1htIVNXU130_provenance;
    np:hasPublicationInfo dgn-np:NP787668.RAnU1GgnyyQccRb7wqae6XZr7WOilKcQn2LuI1htIVNXU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP787668.RAnU1GgnyyQccRb7wqae6XZr7WOilKcQn2LuI1htIVNXU130_assertion a np:Assertion .
  
  dgn-np:NP787668.RAnU1GgnyyQccRb7wqae6XZr7WOilKcQn2LuI1htIVNXU130_provenance a np:Provenance .
  
  dgn-np:NP787668.RAnU1GgnyyQccRb7wqae6XZr7WOilKcQn2LuI1htIVNXU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP787668.RAnU1GgnyyQccRb7wqae6XZr7WOilKcQn2LuI1htIVNXU130_assertion {
  miriam-gene:50987 a ncit:C16612 .
  
  lld:C0014544 a ncit:C7057 .
  
  dgn-gda:DGNb77178bad36cfd7d37bd3f60dec67dda sio:SIO_000628 miriam-gene:50987, lld:C0014544;
    a sio:SIO_001121 .
}

dgn-np:NP787668.RAnU1GgnyyQccRb7wqae6XZr7WOilKcQn2LuI1htIVNXU130_provenance {
  dgn-np:NP787668.RAnU1GgnyyQccRb7wqae6XZr7WOilKcQn2LuI1htIVNXU130_assertion dcterms:description
      "[Familial partial epilepsy with variable foci (FPEVF) is an autosomal dominant form of partial epilepsy characterized by the presence of epileptic seizures originating from different cerebral lobes in different members of the same family.]. 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:20659149;
    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:NP787668.RAnU1GgnyyQccRb7wqae6XZr7WOilKcQn2LuI1htIVNXU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:00+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" .
}