@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP861446.RAme2hV5SDO7s2-Eq2vfmisenaDz9VYBMB0numtokNXtE> .
@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:NP861446.RAme2hV5SDO7s2-Eq2vfmisenaDz9VYBMB0numtokNXtE130_head {
  this: np:hasAssertion dgn-np:NP861446.RAme2hV5SDO7s2-Eq2vfmisenaDz9VYBMB0numtokNXtE130_assertion;
    np:hasProvenance dgn-np:NP861446.RAme2hV5SDO7s2-Eq2vfmisenaDz9VYBMB0numtokNXtE130_provenance;
    np:hasPublicationInfo dgn-np:NP861446.RAme2hV5SDO7s2-Eq2vfmisenaDz9VYBMB0numtokNXtE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP861446.RAme2hV5SDO7s2-Eq2vfmisenaDz9VYBMB0numtokNXtE130_assertion a np:Assertion .
  
  dgn-np:NP861446.RAme2hV5SDO7s2-Eq2vfmisenaDz9VYBMB0numtokNXtE130_provenance a np:Provenance .
  
  dgn-np:NP861446.RAme2hV5SDO7s2-Eq2vfmisenaDz9VYBMB0numtokNXtE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP861446.RAme2hV5SDO7s2-Eq2vfmisenaDz9VYBMB0numtokNXtE130_assertion {
  miriam-gene:11173 a ncit:C16612 .
  
  lld:C0010068 a ncit:C7057 .
  
  dgn-gda:DGN2d821526a9381d6c386aa1f5fe71ca68 sio:SIO_000628 miriam-gene:11173, lld:C0010068;
    a sio:SIO_001122 .
}

dgn-np:NP861446.RAme2hV5SDO7s2-Eq2vfmisenaDz9VYBMB0numtokNXtE130_provenance {
  dgn-np:NP861446.RAme2hV5SDO7s2-Eq2vfmisenaDz9VYBMB0numtokNXtE130_assertion dcterms:description
      "[Recent studies have identified the ABO rs579459, PPAP2B rs17114036, and ADAMTS7 rs3825807 polymorphisms as genetic variants associated with coronary artery disease and the PIK3CG rs17398575 and EDNRA rs1878406 polymorphisms as the most significant signals related to the presence of carotid plaque in nonrheumatic Caucasian individuals.]. 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:24795506;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP861446.RAme2hV5SDO7s2-Eq2vfmisenaDz9VYBMB0numtokNXtE130_publicationInfo {
  this: dcterms:created "2015-08-25T14:46:23+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}