@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP705091.RAwdT1_BVb2oitw7JDfKkIX9prgm3NA4MbbWsRz5351kk> .
@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:NP705091.RAwdT1_BVb2oitw7JDfKkIX9prgm3NA4MbbWsRz5351kk130_head {
  this: np:hasAssertion dgn-np:NP705091.RAwdT1_BVb2oitw7JDfKkIX9prgm3NA4MbbWsRz5351kk130_assertion;
    np:hasProvenance dgn-np:NP705091.RAwdT1_BVb2oitw7JDfKkIX9prgm3NA4MbbWsRz5351kk130_provenance;
    np:hasPublicationInfo dgn-np:NP705091.RAwdT1_BVb2oitw7JDfKkIX9prgm3NA4MbbWsRz5351kk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP705091.RAwdT1_BVb2oitw7JDfKkIX9prgm3NA4MbbWsRz5351kk130_assertion a np:Assertion .
  
  dgn-np:NP705091.RAwdT1_BVb2oitw7JDfKkIX9prgm3NA4MbbWsRz5351kk130_provenance a np:Provenance .
  
  dgn-np:NP705091.RAwdT1_BVb2oitw7JDfKkIX9prgm3NA4MbbWsRz5351kk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP705091.RAwdT1_BVb2oitw7JDfKkIX9prgm3NA4MbbWsRz5351kk130_assertion {
  miriam-gene:5649 a ncit:C16612 .
  
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dgn-np:NP705091.RAwdT1_BVb2oitw7JDfKkIX9prgm3NA4MbbWsRz5351kk130_provenance {
  dgn-np:NP705091.RAwdT1_BVb2oitw7JDfKkIX9prgm3NA4MbbWsRz5351kk130_assertion dcterms:description
      "[We studied immunohistochemically 30 cases of focal cortical dysplasia (FCD) type IIIa to verify whether Reelin could represent the pathogenetic link between HS and cortical dyslamination in the setting of FCD type IIIa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
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    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 .
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dgn-np:NP705091.RAwdT1_BVb2oitw7JDfKkIX9prgm3NA4MbbWsRz5351kk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:08+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;
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