@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP682215.RAyjBwmIauUMJ5y_qyup8bx7g8f8HiA8382S8zQK3pgH8> .
@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:NP682215.RAyjBwmIauUMJ5y_qyup8bx7g8f8HiA8382S8zQK3pgH8130_head {
  this: np:hasAssertion dgn-np:NP682215.RAyjBwmIauUMJ5y_qyup8bx7g8f8HiA8382S8zQK3pgH8130_assertion;
    np:hasProvenance dgn-np:NP682215.RAyjBwmIauUMJ5y_qyup8bx7g8f8HiA8382S8zQK3pgH8130_provenance;
    np:hasPublicationInfo dgn-np:NP682215.RAyjBwmIauUMJ5y_qyup8bx7g8f8HiA8382S8zQK3pgH8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP682215.RAyjBwmIauUMJ5y_qyup8bx7g8f8HiA8382S8zQK3pgH8130_assertion a np:Assertion .
  
  dgn-np:NP682215.RAyjBwmIauUMJ5y_qyup8bx7g8f8HiA8382S8zQK3pgH8130_provenance a np:Provenance .
  
  dgn-np:NP682215.RAyjBwmIauUMJ5y_qyup8bx7g8f8HiA8382S8zQK3pgH8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP682215.RAyjBwmIauUMJ5y_qyup8bx7g8f8HiA8382S8zQK3pgH8130_assertion {
  miriam-gene:6319 a ncit:C16612 .
  
  lld:C0010068 a ncit:C7057 .
  
  dgn-gda:DGN6dedd57245e22de174c4a9bf2c677864 sio:SIO_000628 miriam-gene:6319, lld:C0010068;
    a sio:SIO_001121 .
}

dgn-np:NP682215.RAyjBwmIauUMJ5y_qyup8bx7g8f8HiA8382S8zQK3pgH8130_provenance {
  dgn-np:NP682215.RAyjBwmIauUMJ5y_qyup8bx7g8f8HiA8382S8zQK3pgH8130_assertion dcterms:description
      "[It is becoming increasingly appreciated that besides depressed left ventricular systolic function and the conventional risk stratification tools, new markers for plaque vulnerability, enhanced thrombogenesis, specific genetic alterations of the autonomic nervous system, cardiac sarcolemmal and contractile proteins, and familial clustering may better segregate patients with atherosclerotic coronary artery disease who are at high risk for SCD from those who may suffer from nonfatal ischemic events.]. 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:14521667;
    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:NP682215.RAyjBwmIauUMJ5y_qyup8bx7g8f8HiA8382S8zQK3pgH8130_publicationInfo {
  this: dcterms:created "2015-08-25T14:44:31+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" .
}