@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP303978.RAVT2vnS_fdSmb6AIRzndrV530Fz7MZym4y59cia-A7lo> .
@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:NP303978.RAVT2vnS_fdSmb6AIRzndrV530Fz7MZym4y59cia-A7lo130_head {
  this: np:hasAssertion dgn-np:NP303978.RAVT2vnS_fdSmb6AIRzndrV530Fz7MZym4y59cia-A7lo130_assertion;
    np:hasProvenance dgn-np:NP303978.RAVT2vnS_fdSmb6AIRzndrV530Fz7MZym4y59cia-A7lo130_provenance;
    np:hasPublicationInfo dgn-np:NP303978.RAVT2vnS_fdSmb6AIRzndrV530Fz7MZym4y59cia-A7lo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP303978.RAVT2vnS_fdSmb6AIRzndrV530Fz7MZym4y59cia-A7lo130_assertion a np:Assertion .
  
  dgn-np:NP303978.RAVT2vnS_fdSmb6AIRzndrV530Fz7MZym4y59cia-A7lo130_provenance a np:Provenance .
  
  dgn-np:NP303978.RAVT2vnS_fdSmb6AIRzndrV530Fz7MZym4y59cia-A7lo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP303978.RAVT2vnS_fdSmb6AIRzndrV530Fz7MZym4y59cia-A7lo130_assertion {
  miriam-gene:3240 a ncit:C16612 .
  
  lld:C0333186 a ncit:C7057 .
  
  dgn-gda:DGNa82c37181acae0fcc556d6200484fed8 sio:SIO_000628 miriam-gene:3240, lld:C0333186;
    a sio:SIO_001121 .
}

dgn-np:NP303978.RAVT2vnS_fdSmb6AIRzndrV530Fz7MZym4y59cia-A7lo130_provenance {
  dgn-np:NP303978.RAVT2vnS_fdSmb6AIRzndrV530Fz7MZym4y59cia-A7lo130_assertion dcterms:description
      "[The goal of this study was to determine whether the haptoglobin (Hp) genotype was predictive of restenosis and major adverse cardiac events (MACEs) after percutaneous transluminal coronary angioplasty (PTCA) in individuals with diabetes.]. 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:12941730;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP303978.RAVT2vnS_fdSmb6AIRzndrV530Fz7MZym4y59cia-A7lo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:54+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}