@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP350376.RAGjG0U_mnFVGkJyUmhJdRb03Mgn4wrrCgLWXBVXooxBs> .
@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:NP350376.RAGjG0U_mnFVGkJyUmhJdRb03Mgn4wrrCgLWXBVXooxBs130_head {
  this: np:hasAssertion dgn-np:NP350376.RAGjG0U_mnFVGkJyUmhJdRb03Mgn4wrrCgLWXBVXooxBs130_assertion;
    np:hasProvenance dgn-np:NP350376.RAGjG0U_mnFVGkJyUmhJdRb03Mgn4wrrCgLWXBVXooxBs130_provenance;
    np:hasPublicationInfo dgn-np:NP350376.RAGjG0U_mnFVGkJyUmhJdRb03Mgn4wrrCgLWXBVXooxBs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP350376.RAGjG0U_mnFVGkJyUmhJdRb03Mgn4wrrCgLWXBVXooxBs130_assertion a np:Assertion .
  
  dgn-np:NP350376.RAGjG0U_mnFVGkJyUmhJdRb03Mgn4wrrCgLWXBVXooxBs130_provenance a np:Provenance .
  
  dgn-np:NP350376.RAGjG0U_mnFVGkJyUmhJdRb03Mgn4wrrCgLWXBVXooxBs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP350376.RAGjG0U_mnFVGkJyUmhJdRb03Mgn4wrrCgLWXBVXooxBs130_assertion {
  miriam-gene:63973 a ncit:C16612 .
  
  lld:C0014544 a ncit:C7057 .
  
  dgn-gda:DGN6995ca83322a3c698e95b3238f536332 sio:SIO_000628 miriam-gene:63973, lld:C0014544;
    a sio:SIO_001121 .
}

dgn-np:NP350376.RAGjG0U_mnFVGkJyUmhJdRb03Mgn4wrrCgLWXBVXooxBs130_provenance {
  dgn-np:NP350376.RAGjG0U_mnFVGkJyUmhJdRb03Mgn4wrrCgLWXBVXooxBs130_assertion dcterms:description
      "[The genes NEUROG2, ANK2, UGT8 and CAMK2D, which are known to be expressed in human brain, are strong positional candidates and we propose to examine these and other genes in the locus to identify the causative gene for this intriguing form of epilepsy.]. 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:19597845;
    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:NP350376.RAGjG0U_mnFVGkJyUmhJdRb03Mgn4wrrCgLWXBVXooxBs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:25+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}