@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1063421.RARYbg3CJNeFcyfFCuvK4t_MSd943fazWpuScVi9XCZxc> .
@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/v4.0.0/void/> .

dgn-np:NP1063421.RARYbg3CJNeFcyfFCuvK4t_MSd943fazWpuScVi9XCZxc130_head {
  this: np:hasAssertion dgn-np:NP1063421.RARYbg3CJNeFcyfFCuvK4t_MSd943fazWpuScVi9XCZxc130_assertion;
    np:hasProvenance dgn-np:NP1063421.RARYbg3CJNeFcyfFCuvK4t_MSd943fazWpuScVi9XCZxc130_provenance;
    np:hasPublicationInfo dgn-np:NP1063421.RARYbg3CJNeFcyfFCuvK4t_MSd943fazWpuScVi9XCZxc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1063421.RARYbg3CJNeFcyfFCuvK4t_MSd943fazWpuScVi9XCZxc130_assertion a np:Assertion .
  
  dgn-np:NP1063421.RARYbg3CJNeFcyfFCuvK4t_MSd943fazWpuScVi9XCZxc130_provenance a np:Provenance .
  
  dgn-np:NP1063421.RARYbg3CJNeFcyfFCuvK4t_MSd943fazWpuScVi9XCZxc130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1063421.RARYbg3CJNeFcyfFCuvK4t_MSd943fazWpuScVi9XCZxc130_assertion {
  miriam-gene:790 a ncit:C16612 .
  
  lld:C0018801 a ncit:C7057 .
  
  dgn-gda:DGN03aed49749af2111ad9709d5bbd204a9 sio:SIO_000628 miriam-gene:790, lld:C0018801;
    a sio:SIO_001121 .
}

dgn-np:NP1063421.RARYbg3CJNeFcyfFCuvK4t_MSd943fazWpuScVi9XCZxc130_provenance {
  dgn-np:NP1063421.RARYbg3CJNeFcyfFCuvK4t_MSd943fazWpuScVi9XCZxc130_assertion dcterms:description
      "[In addition, differences in the allelic and the genotypic frequencies of homozygous genotypes were found between the HF patients free from evidence of coronary significant lesions and patients with at least one hemodynamically significant coronary lesion, both HF and 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:23527722;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1063421.RARYbg3CJNeFcyfFCuvK4t_MSd943fazWpuScVi9XCZxc130_publicationInfo {
  this: dcterms:created "2016-05-13T12:49:48+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}