@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP87079.RArWlETfAHloMapBwoNnwVQ6LI4h2ihry_zFcWAGumurU> .
@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:NP87079.RArWlETfAHloMapBwoNnwVQ6LI4h2ihry_zFcWAGumurU130_head {
  this: np:hasAssertion dgn-np:NP87079.RArWlETfAHloMapBwoNnwVQ6LI4h2ihry_zFcWAGumurU130_assertion;
    np:hasProvenance dgn-np:NP87079.RArWlETfAHloMapBwoNnwVQ6LI4h2ihry_zFcWAGumurU130_provenance;
    np:hasPublicationInfo dgn-np:NP87079.RArWlETfAHloMapBwoNnwVQ6LI4h2ihry_zFcWAGumurU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP87079.RArWlETfAHloMapBwoNnwVQ6LI4h2ihry_zFcWAGumurU130_assertion a np:Assertion .
  
  dgn-np:NP87079.RArWlETfAHloMapBwoNnwVQ6LI4h2ihry_zFcWAGumurU130_provenance a np:Provenance .
  
  dgn-np:NP87079.RArWlETfAHloMapBwoNnwVQ6LI4h2ihry_zFcWAGumurU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP87079.RArWlETfAHloMapBwoNnwVQ6LI4h2ihry_zFcWAGumurU130_assertion {
  miriam-gene:2811 a ncit:C16612 .
  
  lld:C0004153 a ncit:C7057 .
  
  dgn-gda:DGN8d469060df39bb03487e55f846e8747b sio:SIO_000628 miriam-gene:2811, lld:C0004153;
    a sio:SIO_001122 .
}

dgn-np:NP87079.RArWlETfAHloMapBwoNnwVQ6LI4h2ihry_zFcWAGumurU130_provenance {
  dgn-np:NP87079.RArWlETfAHloMapBwoNnwVQ6LI4h2ihry_zFcWAGumurU130_assertion dcterms:description
      "[, the 807T allele of GP Ia and the PlA2 allele of GP IIIa, and specially its combination, may confer an additional risk for development of carotid atherosclerosis and arterial thrombosis in type 2 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:20076847;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP87079.RArWlETfAHloMapBwoNnwVQ6LI4h2ihry_zFcWAGumurU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:43+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" .
}