@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP224164.RArCq9mCYiKsxvkIf1N_dpkxQP74uDoMjpxfSI1uutjSY> .
@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:NP224164.RArCq9mCYiKsxvkIf1N_dpkxQP74uDoMjpxfSI1uutjSY130_head {
  this: np:hasAssertion dgn-np:NP224164.RArCq9mCYiKsxvkIf1N_dpkxQP74uDoMjpxfSI1uutjSY130_assertion;
    np:hasProvenance dgn-np:NP224164.RArCq9mCYiKsxvkIf1N_dpkxQP74uDoMjpxfSI1uutjSY130_provenance;
    np:hasPublicationInfo dgn-np:NP224164.RArCq9mCYiKsxvkIf1N_dpkxQP74uDoMjpxfSI1uutjSY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP224164.RArCq9mCYiKsxvkIf1N_dpkxQP74uDoMjpxfSI1uutjSY130_assertion a np:Assertion .
  
  dgn-np:NP224164.RArCq9mCYiKsxvkIf1N_dpkxQP74uDoMjpxfSI1uutjSY130_provenance a np:Provenance .
  
  dgn-np:NP224164.RArCq9mCYiKsxvkIf1N_dpkxQP74uDoMjpxfSI1uutjSY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP224164.RArCq9mCYiKsxvkIf1N_dpkxQP74uDoMjpxfSI1uutjSY130_assertion {
  miriam-gene:1636 a ncit:C16612 .
  
  lld:C0333186 a ncit:C7057 .
  
  dgn-gda:DGN2a54e46845976a71bfc6de1d1a5a148d sio:SIO_000628 miriam-gene:1636, lld:C0333186;
    a sio:SIO_001121 .
}

dgn-np:NP224164.RArCq9mCYiKsxvkIf1N_dpkxQP74uDoMjpxfSI1uutjSY130_provenance {
  dgn-np:NP224164.RArCq9mCYiKsxvkIf1N_dpkxQP74uDoMjpxfSI1uutjSY130_assertion dcterms:description
      "[In humans, a strong correlation has been found between plasma angiotensin I-converting enzyme (ACE) activity and the insertion/deletion (I/D) polymorphism of the ACE gene, which has been reported to be associated with myocardial infarction, ischemic and idiopathic dilated cardiomyopathy, sudden death in hypertrophic cardiomyopathy, and restenosis after percutaneous transluminal coronary angioplasty.]. 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:7994801;
    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:NP224164.RArCq9mCYiKsxvkIf1N_dpkxQP74uDoMjpxfSI1uutjSY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:04+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" .
}