@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP139997.RAMhDtslsXxbPSJ1ZLl_3Aj_VBkl1JVo2mFcNjW4QEBvQ> .
@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:NP139997.RAMhDtslsXxbPSJ1ZLl_3Aj_VBkl1JVo2mFcNjW4QEBvQ130_head {
  this: np:hasAssertion dgn-np:NP139997.RAMhDtslsXxbPSJ1ZLl_3Aj_VBkl1JVo2mFcNjW4QEBvQ130_assertion;
    np:hasProvenance dgn-np:NP139997.RAMhDtslsXxbPSJ1ZLl_3Aj_VBkl1JVo2mFcNjW4QEBvQ130_provenance;
    np:hasPublicationInfo dgn-np:NP139997.RAMhDtslsXxbPSJ1ZLl_3Aj_VBkl1JVo2mFcNjW4QEBvQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP139997.RAMhDtslsXxbPSJ1ZLl_3Aj_VBkl1JVo2mFcNjW4QEBvQ130_assertion a np:Assertion .
  
  dgn-np:NP139997.RAMhDtslsXxbPSJ1ZLl_3Aj_VBkl1JVo2mFcNjW4QEBvQ130_provenance a np:Provenance .
  
  dgn-np:NP139997.RAMhDtslsXxbPSJ1ZLl_3Aj_VBkl1JVo2mFcNjW4QEBvQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP139997.RAMhDtslsXxbPSJ1ZLl_3Aj_VBkl1JVo2mFcNjW4QEBvQ130_assertion {
  miriam-gene:1535 a ncit:C16612 .
  
  lld:C0242231 a ncit:C7057 .
  
  dgn-gda:DGNe651d24a1e5912f2e112fef08eb74586 sio:SIO_000628 miriam-gene:1535, lld:C0242231;
    a sio:SIO_001121 .
}

dgn-np:NP139997.RAMhDtslsXxbPSJ1ZLl_3Aj_VBkl1JVo2mFcNjW4QEBvQ130_provenance {
  dgn-np:NP139997.RAMhDtslsXxbPSJ1ZLl_3Aj_VBkl1JVo2mFcNjW4QEBvQ130_assertion dcterms:description
      "[These results support the increased risk of developing early coronary artery disease and of having rapid progression of coronary stenosis in subjects carrying the C242T nucleotide transition among the Italian population.]. 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:16788250;
    prov:wasDerivedFrom dgn-void:lhgdn-20090331;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:lhgdn-20090331 pav:importedOn "2009-03-31"^^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:NP139997.RAMhDtslsXxbPSJ1ZLl_3Aj_VBkl1JVo2mFcNjW4QEBvQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:13+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" .
}