@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP63527.RAUeBv1KdiY8_jYnvUH74mC-kz7nYEIK9DJ0-TLP82UF0> .
@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:NP63527.RAUeBv1KdiY8_jYnvUH74mC-kz7nYEIK9DJ0-TLP82UF0130_head {
  this: np:hasAssertion dgn-np:NP63527.RAUeBv1KdiY8_jYnvUH74mC-kz7nYEIK9DJ0-TLP82UF0130_assertion;
    np:hasProvenance dgn-np:NP63527.RAUeBv1KdiY8_jYnvUH74mC-kz7nYEIK9DJ0-TLP82UF0130_provenance;
    np:hasPublicationInfo dgn-np:NP63527.RAUeBv1KdiY8_jYnvUH74mC-kz7nYEIK9DJ0-TLP82UF0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP63527.RAUeBv1KdiY8_jYnvUH74mC-kz7nYEIK9DJ0-TLP82UF0130_assertion a np:Assertion .
  
  dgn-np:NP63527.RAUeBv1KdiY8_jYnvUH74mC-kz7nYEIK9DJ0-TLP82UF0130_provenance a np:Provenance .
  
  dgn-np:NP63527.RAUeBv1KdiY8_jYnvUH74mC-kz7nYEIK9DJ0-TLP82UF0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP63527.RAUeBv1KdiY8_jYnvUH74mC-kz7nYEIK9DJ0-TLP82UF0130_assertion {
  miriam-gene:125 a ncit:C16612 .
  
  lld:C0010054 a ncit:C7057 .
  
  dgn-gda:DGN531d43097a7bb3203163172c2278a1a4 sio:SIO_000628 miriam-gene:125, lld:C0010054;
    a sio:SIO_001122 .
}

dgn-np:NP63527.RAUeBv1KdiY8_jYnvUH74mC-kz7nYEIK9DJ0-TLP82UF0130_provenance {
  dgn-np:NP63527.RAUeBv1KdiY8_jYnvUH74mC-kz7nYEIK9DJ0-TLP82UF0130_assertion dcterms:description
      "[The mutant genotypes of eNOS gene T-786C mutation and the fast form of ADH2 Arg47His polymorphism had an additive interaction on the risk of premature CAD in Chinese population. Further investigations with big sample size are necessary for confirming this additive interaction.]. 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:17289126;
    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:NP63527.RAUeBv1KdiY8_jYnvUH74mC-kz7nYEIK9DJ0-TLP82UF0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:30+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" .
}