@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP436031.RAFH4JmWpTtn8_WVCgdQLbxAsP1fE3a5fNXc8fwLzTa78> .
@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:NP436031.RAFH4JmWpTtn8_WVCgdQLbxAsP1fE3a5fNXc8fwLzTa78130_head {
  this: np:hasAssertion dgn-np:NP436031.RAFH4JmWpTtn8_WVCgdQLbxAsP1fE3a5fNXc8fwLzTa78130_assertion;
    np:hasProvenance dgn-np:NP436031.RAFH4JmWpTtn8_WVCgdQLbxAsP1fE3a5fNXc8fwLzTa78130_provenance;
    np:hasPublicationInfo dgn-np:NP436031.RAFH4JmWpTtn8_WVCgdQLbxAsP1fE3a5fNXc8fwLzTa78130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP436031.RAFH4JmWpTtn8_WVCgdQLbxAsP1fE3a5fNXc8fwLzTa78130_assertion a np:Assertion .
  
  dgn-np:NP436031.RAFH4JmWpTtn8_WVCgdQLbxAsP1fE3a5fNXc8fwLzTa78130_provenance a np:Provenance .
  
  dgn-np:NP436031.RAFH4JmWpTtn8_WVCgdQLbxAsP1fE3a5fNXc8fwLzTa78130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP436031.RAFH4JmWpTtn8_WVCgdQLbxAsP1fE3a5fNXc8fwLzTa78130_assertion {
  miriam-gene:6387 a ncit:C16612 .
  
  lld:C0010054 a ncit:C7057 .
  
  dgn-gda:DGN83d6dfe6669fd5daa816016b7f884a31 sio:SIO_000628 miriam-gene:6387, lld:C0010054;
    a sio:SIO_001121 .
}

dgn-np:NP436031.RAFH4JmWpTtn8_WVCgdQLbxAsP1fE3a5fNXc8fwLzTa78130_provenance {
  dgn-np:NP436031.RAFH4JmWpTtn8_WVCgdQLbxAsP1fE3a5fNXc8fwLzTa78130_assertion dcterms:description
      "[Because previous genome-wide association studies demonstrated an association between CXCL12 rs501120 and coronary artery disease, in the present study we assessed the potential association of this polymorphism with the risk of cardiovascular (CV) disease in 1,321 Spanish patients with RA.]. 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:22386691;
    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:NP436031.RAFH4JmWpTtn8_WVCgdQLbxAsP1fE3a5fNXc8fwLzTa78130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:18+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" .
}