@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP61637.RA7__6WQEV9_yLQ3KnbI6TknrmopzQfVjn0eszLVCm8AQ> .
@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:NP61637.RA7__6WQEV9_yLQ3KnbI6TknrmopzQfVjn0eszLVCm8AQ130_head {
  this: np:hasAssertion dgn-np:NP61637.RA7__6WQEV9_yLQ3KnbI6TknrmopzQfVjn0eszLVCm8AQ130_assertion;
    np:hasProvenance dgn-np:NP61637.RA7__6WQEV9_yLQ3KnbI6TknrmopzQfVjn0eszLVCm8AQ130_provenance;
    np:hasPublicationInfo dgn-np:NP61637.RA7__6WQEV9_yLQ3KnbI6TknrmopzQfVjn0eszLVCm8AQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP61637.RA7__6WQEV9_yLQ3KnbI6TknrmopzQfVjn0eszLVCm8AQ130_assertion a np:Assertion .
  
  dgn-np:NP61637.RA7__6WQEV9_yLQ3KnbI6TknrmopzQfVjn0eszLVCm8AQ130_provenance a np:Provenance .
  
  dgn-np:NP61637.RA7__6WQEV9_yLQ3KnbI6TknrmopzQfVjn0eszLVCm8AQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP61637.RA7__6WQEV9_yLQ3KnbI6TknrmopzQfVjn0eszLVCm8AQ130_assertion {
  miriam-gene:4846 a ncit:C16612 .
  
  lld:C0004096 a ncit:C7057 .
  
  dgn-gda:DGN69d463f906ed96067f34140e2aad163c sio:SIO_000628 miriam-gene:4846, lld:C0004096;
    a sio:SIO_001122 .
}

dgn-np:NP61637.RA7__6WQEV9_yLQ3KnbI6TknrmopzQfVjn0eszLVCm8AQ130_provenance {
  dgn-np:NP61637.RA7__6WQEV9_yLQ3KnbI6TknrmopzQfVjn0eszLVCm8AQ130_assertion dcterms:description
      "[ T allele had been described as susceptibility allele for CAD in several population studies. The frequency of the T allele was found to be two times higher in our subjects than that reported for Japanese and Korean populations. This study does not provide any direct evidence for eNOS gene disease associations but is the first report on the prevalence of eNOS Glu298Asp gene polymorphism in Indian subjects. Whether the observed pattern of eNOS Glu298Asp polymorphism contributes to the greater susceptibility of Asian Indians to CAD as compared to the other population groups, needs to be investigated.]. 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:16113535;
    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:NP61637.RA7__6WQEV9_yLQ3KnbI6TknrmopzQfVjn0eszLVCm8AQ130_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" .
}