@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1321383.RARC_DgDY1YBwinWXGJ11hfA-lLIH2sTKv7Gplq8Q6awM> .
@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:NP1321383.RARC_DgDY1YBwinWXGJ11hfA-lLIH2sTKv7Gplq8Q6awM130_head {
  this: np:hasAssertion dgn-np:NP1321383.RARC_DgDY1YBwinWXGJ11hfA-lLIH2sTKv7Gplq8Q6awM130_assertion ;
    np:hasProvenance dgn-np:NP1321383.RARC_DgDY1YBwinWXGJ11hfA-lLIH2sTKv7Gplq8Q6awM130_provenance ;
    np:hasPublicationInfo dgn-np:NP1321383.RARC_DgDY1YBwinWXGJ11hfA-lLIH2sTKv7Gplq8Q6awM130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP1321383.RARC_DgDY1YBwinWXGJ11hfA-lLIH2sTKv7Gplq8Q6awM130_assertion a np:Assertion .
  dgn-np:NP1321383.RARC_DgDY1YBwinWXGJ11hfA-lLIH2sTKv7Gplq8Q6awM130_provenance a np:Provenance .
  dgn-np:NP1321383.RARC_DgDY1YBwinWXGJ11hfA-lLIH2sTKv7Gplq8Q6awM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP1321383.RARC_DgDY1YBwinWXGJ11hfA-lLIH2sTKv7Gplq8Q6awM130_assertion {
  miriam-gene:1636 a ncit:C16612 .
  lld:C0878544 a ncit:C7057 .
  dgn-gda:DGN8a818fa50326e343e4926aee38ba9751 sio:SIO_000628 miriam-gene:1636 , lld:C0878544 ;
    a sio:SIO_001121 .
}
dgn-np:NP1321383.RARC_DgDY1YBwinWXGJ11hfA-lLIH2sTKv7Gplq8Q6awM130_provenance {
  dgn-np:NP1321383.RARC_DgDY1YBwinWXGJ11hfA-lLIH2sTKv7Gplq8Q6awM130_assertion dcterms:description "[Recent reports have shown that the frequency of the homozygous deletion genotype (DD) of the angiotensin-converting enzyme (ACE) gene is highly associated with myocardial infarction and cardiomyopathy, particularly in those considered to be at low risk for coronary heart disease (CHD) on the basis of their apoB or LDL cholesterol concentrations.]. 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:7773733 ;
    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:NP1321383.RARC_DgDY1YBwinWXGJ11hfA-lLIH2sTKv7Gplq8Q6awM130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:45+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" .
}