@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP61687.RAE_nSNqZ_hsAo_nVycEaxCUaxL_9D22PhR6zMTkCSneY> .
@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:NP61687.RAE_nSNqZ_hsAo_nVycEaxCUaxL_9D22PhR6zMTkCSneY130_head {
  this: np:hasAssertion dgn-np:NP61687.RAE_nSNqZ_hsAo_nVycEaxCUaxL_9D22PhR6zMTkCSneY130_assertion;
    np:hasProvenance dgn-np:NP61687.RAE_nSNqZ_hsAo_nVycEaxCUaxL_9D22PhR6zMTkCSneY130_provenance;
    np:hasPublicationInfo dgn-np:NP61687.RAE_nSNqZ_hsAo_nVycEaxCUaxL_9D22PhR6zMTkCSneY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP61687.RAE_nSNqZ_hsAo_nVycEaxCUaxL_9D22PhR6zMTkCSneY130_assertion a np:Assertion .
  
  dgn-np:NP61687.RAE_nSNqZ_hsAo_nVycEaxCUaxL_9D22PhR6zMTkCSneY130_provenance a np:Provenance .
  
  dgn-np:NP61687.RAE_nSNqZ_hsAo_nVycEaxCUaxL_9D22PhR6zMTkCSneY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP61687.RAE_nSNqZ_hsAo_nVycEaxCUaxL_9D22PhR6zMTkCSneY130_assertion {
  miriam-gene:4846 a ncit:C16612 .
  
  lld:C0027051 a ncit:C7057 .
  
  dgn-gda:DGN4c8db4029ffd006784aeaa1710f5c6b3 sio:SIO_000628 miriam-gene:4846, lld:C0027051;
    a sio:SIO_001122 .
}

dgn-np:NP61687.RAE_nSNqZ_hsAo_nVycEaxCUaxL_9D22PhR6zMTkCSneY130_provenance {
  dgn-np:NP61687.RAE_nSNqZ_hsAo_nVycEaxCUaxL_9D22PhR6zMTkCSneY130_assertion dcterms:description
      "[This study indicates that E298D polymorphism of the eNOS gene seems to be associated with MI occurrence in the Greek population. It is possible that TT genotype is closely linked to the etiology of MI even after adjusting for known MI risk factors.]. 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:20854685;
    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:NP61687.RAE_nSNqZ_hsAo_nVycEaxCUaxL_9D22PhR6zMTkCSneY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:29+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" .
}