@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1008558.RA2Y1xdQ5o8oxsf1zLCHoVn3hnWQWoWRu60ZbG3vBjJJg> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .
dgn-np:NP1008558.RA2Y1xdQ5o8oxsf1zLCHoVn3hnWQWoWRu60ZbG3vBjJJg130_head {
  this: np:hasAssertion dgn-np:NP1008558.RA2Y1xdQ5o8oxsf1zLCHoVn3hnWQWoWRu60ZbG3vBjJJg130_assertion ;
    np:hasProvenance dgn-np:NP1008558.RA2Y1xdQ5o8oxsf1zLCHoVn3hnWQWoWRu60ZbG3vBjJJg130_provenance ;
    np:hasPublicationInfo dgn-np:NP1008558.RA2Y1xdQ5o8oxsf1zLCHoVn3hnWQWoWRu60ZbG3vBjJJg130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP1008558.RA2Y1xdQ5o8oxsf1zLCHoVn3hnWQWoWRu60ZbG3vBjJJg130_assertion a np:Assertion .
  dgn-np:NP1008558.RA2Y1xdQ5o8oxsf1zLCHoVn3hnWQWoWRu60ZbG3vBjJJg130_provenance a np:Provenance .
  dgn-np:NP1008558.RA2Y1xdQ5o8oxsf1zLCHoVn3hnWQWoWRu60ZbG3vBjJJg130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP1008558.RA2Y1xdQ5o8oxsf1zLCHoVn3hnWQWoWRu60ZbG3vBjJJg130_assertion {
  miriam-gene:4524 a ncit:C16612 .
  lld:C0003873 a ncit:C7057 .
  dgn-gda:DGNb4a8e922d539ae7942e03e3fd1f6e210 sio:SIO_000628 miriam-gene:4524 , lld:C0003873 ;
    a sio:SIO_001122 .
}
dgn-np:NP1008558.RA2Y1xdQ5o8oxsf1zLCHoVn3hnWQWoWRu60ZbG3vBjJJg130_provenance {
  dgn-np:NP1008558.RA2Y1xdQ5o8oxsf1zLCHoVn3hnWQWoWRu60ZbG3vBjJJg130_assertion dcterms:description "[In this regard, besides a strong association between the HLA-DRB1∗04 shared epitope alleles and both endothelial dysfunction, an early step in the atherosclerotic process, and clinically evident CV disease, other polymorphisms belonging to genes implicated in inflammatory and metabolic pathways, located inside and outside the HLA region, such as the 308 variant (G &gt; A, rs1800629) of the TNFA locus, the rs1801131 polymorphism (A &gt; C; position + 1298) of the MTHFR locus, or a deletion of 32 base pairs on the CCR5 gene, seem to be associated with the risk of CV disease in 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:22927710 ;
    prov:wasDerivedFrom dgn-void:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1008558.RA2Y1xdQ5o8oxsf1zLCHoVn3hnWQWoWRu60ZbG3vBjJJg130_publicationInfo {
  this: dcterms:created "2016-05-13T12:49:23+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:disgenetv3.0rdf ;
    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 "v4.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}