@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP181984.RAAj9PNyUSOK4BD4b5jGNBCZObviatiGx64b7m5V4MJVc> .
@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:NP181984.RAAj9PNyUSOK4BD4b5jGNBCZObviatiGx64b7m5V4MJVc130_head {
  this: np:hasAssertion dgn-np:NP181984.RAAj9PNyUSOK4BD4b5jGNBCZObviatiGx64b7m5V4MJVc130_assertion;
    np:hasProvenance dgn-np:NP181984.RAAj9PNyUSOK4BD4b5jGNBCZObviatiGx64b7m5V4MJVc130_provenance;
    np:hasPublicationInfo dgn-np:NP181984.RAAj9PNyUSOK4BD4b5jGNBCZObviatiGx64b7m5V4MJVc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP181984.RAAj9PNyUSOK4BD4b5jGNBCZObviatiGx64b7m5V4MJVc130_assertion a np:Assertion .
  
  dgn-np:NP181984.RAAj9PNyUSOK4BD4b5jGNBCZObviatiGx64b7m5V4MJVc130_provenance a np:Provenance .
  
  dgn-np:NP181984.RAAj9PNyUSOK4BD4b5jGNBCZObviatiGx64b7m5V4MJVc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP181984.RAAj9PNyUSOK4BD4b5jGNBCZObviatiGx64b7m5V4MJVc130_assertion {
  miriam-gene:729230 a ncit:C16612 .
  
  lld:C1956346 a ncit:C7057 .
  
  dgn-gda:DGN9d7fe9975fc374d74f8e26e005419c42 sio:SIO_000628 miriam-gene:729230, lld:C1956346;
    a sio:SIO_001121 .
}

dgn-np:NP181984.RAAj9PNyUSOK4BD4b5jGNBCZObviatiGx64b7m5V4MJVc130_provenance {
  dgn-np:NP181984.RAAj9PNyUSOK4BD4b5jGNBCZObviatiGx64b7m5V4MJVc130_assertion dcterms:description
      "[V64Ile polymorphism in CCR2 has been implicated in the manifestation of myocardial infarction in different populations, but data on association of the CCR5 deletion variant in etiology of CAD are conflicting.]. 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:17383752;
    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:NP181984.RAAj9PNyUSOK4BD4b5jGNBCZObviatiGx64b7m5V4MJVc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:38+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" .
}