@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP112631.RAiXwc_16qTPeNE95syXCk3epBXLd09dde_SGXBT5HaVA> .
@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/v3.0.0/void/> .
dgn-np:NP112631.RAiXwc_16qTPeNE95syXCk3epBXLd09dde_SGXBT5HaVA130_head {
  this: np:hasAssertion dgn-np:NP112631.RAiXwc_16qTPeNE95syXCk3epBXLd09dde_SGXBT5HaVA130_assertion ;
    np:hasProvenance dgn-np:NP112631.RAiXwc_16qTPeNE95syXCk3epBXLd09dde_SGXBT5HaVA130_provenance ;
    np:hasPublicationInfo dgn-np:NP112631.RAiXwc_16qTPeNE95syXCk3epBXLd09dde_SGXBT5HaVA130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP112631.RAiXwc_16qTPeNE95syXCk3epBXLd09dde_SGXBT5HaVA130_assertion a np:Assertion .
  dgn-np:NP112631.RAiXwc_16qTPeNE95syXCk3epBXLd09dde_SGXBT5HaVA130_provenance a np:Provenance .
  dgn-np:NP112631.RAiXwc_16qTPeNE95syXCk3epBXLd09dde_SGXBT5HaVA130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP112631.RAiXwc_16qTPeNE95syXCk3epBXLd09dde_SGXBT5HaVA130_assertion {
  miriam-gene:1524 a ncit:C16612 .
  lld:C0027051 a ncit:C7057 .
  dgn-gda:DGN4c1b05cae04c4d60a8b565782645b132 sio:SIO_000628 miriam-gene:1524 , lld:C0027051 ;
    a sio:SIO_001122 .
}
dgn-np:NP112631.RAiXwc_16qTPeNE95syXCk3epBXLd09dde_SGXBT5HaVA130_provenance {
  dgn-np:NP112631.RAiXwc_16qTPeNE95syXCk3epBXLd09dde_SGXBT5HaVA130_assertion dcterms:description "[In the present study the association of CX3CR1 genotypes with CAD and myocardial infarction (MI) was investigated in the Ludwigshafen Risk and Cardiovascular Health (LURIC) cohort, including 3316 individuals in whom cardiovascular disease angiographically has been defined or ruled out.]. 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:19628406 ;
    prov:wasDerivedFrom dgn-void:gad-20150221 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP112631.RAiXwc_16qTPeNE95syXCk3epBXLd09dde_SGXBT5HaVA130_publicationInfo {
  this: dcterms:created "2015-08-25T14:38:42+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 "v3.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}