@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP95719.RAK20eGccTCU3MXgVB8266ArYp6774fasPhXZ3aEjQlo4> .
@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:NP95719.RAK20eGccTCU3MXgVB8266ArYp6774fasPhXZ3aEjQlo4130_head {
  this: np:hasAssertion dgn-np:NP95719.RAK20eGccTCU3MXgVB8266ArYp6774fasPhXZ3aEjQlo4130_assertion;
    np:hasProvenance dgn-np:NP95719.RAK20eGccTCU3MXgVB8266ArYp6774fasPhXZ3aEjQlo4130_provenance;
    np:hasPublicationInfo dgn-np:NP95719.RAK20eGccTCU3MXgVB8266ArYp6774fasPhXZ3aEjQlo4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP95719.RAK20eGccTCU3MXgVB8266ArYp6774fasPhXZ3aEjQlo4130_assertion a np:Assertion .
  
  dgn-np:NP95719.RAK20eGccTCU3MXgVB8266ArYp6774fasPhXZ3aEjQlo4130_provenance a np:Provenance .
  
  dgn-np:NP95719.RAK20eGccTCU3MXgVB8266ArYp6774fasPhXZ3aEjQlo4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP95719.RAK20eGccTCU3MXgVB8266ArYp6774fasPhXZ3aEjQlo4130_assertion {
  miriam-gene:28 a ncit:C16612 .
  
  lld:C0007222 a ncit:C7057 .
  
  dgn-gda:DGN691f8d332c1c3aa4a64d471addd65f1a sio:SIO_000628 miriam-gene:28, lld:C0007222;
    a sio:SIO_001122 .
}

dgn-np:NP95719.RAK20eGccTCU3MXgVB8266ArYp6774fasPhXZ3aEjQlo4130_provenance {
  dgn-np:NP95719.RAK20eGccTCU3MXgVB8266ArYp6774fasPhXZ3aEjQlo4130_assertion dcterms:description
      "[Our findings indicate that specific genetic predispositions promote the development of coronary atherosclerosis whereas others lead to myocardial infarction in the presence of coronary atherosclerosis. The relation to specific CAD phenotypes might modify how novel loci are applied in personalised risk assessment and used in the development of novel therapies for CAD.]. 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:21239051;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP95719.RAK20eGccTCU3MXgVB8266ArYp6774fasPhXZ3aEjQlo4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:47+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" .
}