@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP61812.RAYxr_BimCWIzrkMPqOx_Od46501QSuF6ibFF3JiJYOZw> .
@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:NP61812.RAYxr_BimCWIzrkMPqOx_Od46501QSuF6ibFF3JiJYOZw130_head {
  this: np:hasAssertion dgn-np:NP61812.RAYxr_BimCWIzrkMPqOx_Od46501QSuF6ibFF3JiJYOZw130_assertion;
    np:hasProvenance dgn-np:NP61812.RAYxr_BimCWIzrkMPqOx_Od46501QSuF6ibFF3JiJYOZw130_provenance;
    np:hasPublicationInfo dgn-np:NP61812.RAYxr_BimCWIzrkMPqOx_Od46501QSuF6ibFF3JiJYOZw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP61812.RAYxr_BimCWIzrkMPqOx_Od46501QSuF6ibFF3JiJYOZw130_assertion a np:Assertion .
  
  dgn-np:NP61812.RAYxr_BimCWIzrkMPqOx_Od46501QSuF6ibFF3JiJYOZw130_provenance a np:Provenance .
  
  dgn-np:NP61812.RAYxr_BimCWIzrkMPqOx_Od46501QSuF6ibFF3JiJYOZw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP61812.RAYxr_BimCWIzrkMPqOx_Od46501QSuF6ibFF3JiJYOZw130_assertion {
  miriam-gene:4846 a ncit:C16612 .
  
  lld:C0007222 a ncit:C7057 .
  
  dgn-gda:DGN0ff79f660b21596f78943a0c8c0a3e52 sio:SIO_000628 miriam-gene:4846, lld:C0007222;
    a sio:SIO_001122 .
}

dgn-np:NP61812.RAYxr_BimCWIzrkMPqOx_Od46501QSuF6ibFF3JiJYOZw130_provenance {
  dgn-np:NP61812.RAYxr_BimCWIzrkMPqOx_Od46501QSuF6ibFF3JiJYOZw130_assertion dcterms:description
      "[Thus, in the Moscow population the ecNOS4a/4b VNTR of the NOS3 gene and the A1166C polymorphism of the AT1 gene are associated with the IHD development. Furthermore, the correlation with the IHD revealed was much stronger for the NOS3 VNTR locus.]. 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:11190479;
    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:NP61812.RAYxr_BimCWIzrkMPqOx_Od46501QSuF6ibFF3JiJYOZw130_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" .
}