@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP233770.RAEMRQFQ9En8LZG0DDe7sBZojtFYet2UWj-7BxLSAJQvk> .
@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:NP233770.RAEMRQFQ9En8LZG0DDe7sBZojtFYet2UWj-7BxLSAJQvk130_head {
  this: np:hasAssertion dgn-np:NP233770.RAEMRQFQ9En8LZG0DDe7sBZojtFYet2UWj-7BxLSAJQvk130_assertion;
    np:hasProvenance dgn-np:NP233770.RAEMRQFQ9En8LZG0DDe7sBZojtFYet2UWj-7BxLSAJQvk130_provenance;
    np:hasPublicationInfo dgn-np:NP233770.RAEMRQFQ9En8LZG0DDe7sBZojtFYet2UWj-7BxLSAJQvk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP233770.RAEMRQFQ9En8LZG0DDe7sBZojtFYet2UWj-7BxLSAJQvk130_assertion a np:Assertion .
  
  dgn-np:NP233770.RAEMRQFQ9En8LZG0DDe7sBZojtFYet2UWj-7BxLSAJQvk130_provenance a np:Provenance .
  
  dgn-np:NP233770.RAEMRQFQ9En8LZG0DDe7sBZojtFYet2UWj-7BxLSAJQvk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP233770.RAEMRQFQ9En8LZG0DDe7sBZojtFYet2UWj-7BxLSAJQvk130_assertion {
  miriam-gene:958 a ncit:C16612 .
  
  lld:C0007785 a ncit:C7057 .
  
  dgn-gda:DGN9e9bd19ead2a65d648b446a6ce51a644 sio:SIO_000628 miriam-gene:958, lld:C0007785;
    a sio:SIO_001121 .
}

dgn-np:NP233770.RAEMRQFQ9En8LZG0DDe7sBZojtFYet2UWj-7BxLSAJQvk130_provenance {
  dgn-np:NP233770.RAEMRQFQ9En8LZG0DDe7sBZojtFYet2UWj-7BxLSAJQvk130_assertion dcterms:description
      "[This study aims to determine whether functional polymorphism of CD40 is associated with the cerebral infarction (CI) susceptibility, and to investigate the effect of CD40 gene polymorphism on CD40 mRNA expression in PBMCs and plasma sCD40L concentration.]. 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:23669336;
    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:NP233770.RAEMRQFQ9En8LZG0DDe7sBZojtFYet2UWj-7BxLSAJQvk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:11+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" .
}