@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP61676.RAFVazj2MuKGZdfHzLvEY0oCmI44XqelEMngQMeh_gGZ0> .
@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:NP61676.RAFVazj2MuKGZdfHzLvEY0oCmI44XqelEMngQMeh_gGZ0130_head {
  this: np:hasAssertion dgn-np:NP61676.RAFVazj2MuKGZdfHzLvEY0oCmI44XqelEMngQMeh_gGZ0130_assertion;
    np:hasProvenance dgn-np:NP61676.RAFVazj2MuKGZdfHzLvEY0oCmI44XqelEMngQMeh_gGZ0130_provenance;
    np:hasPublicationInfo dgn-np:NP61676.RAFVazj2MuKGZdfHzLvEY0oCmI44XqelEMngQMeh_gGZ0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP61676.RAFVazj2MuKGZdfHzLvEY0oCmI44XqelEMngQMeh_gGZ0130_assertion a np:Assertion .
  
  dgn-np:NP61676.RAFVazj2MuKGZdfHzLvEY0oCmI44XqelEMngQMeh_gGZ0130_provenance a np:Provenance .
  
  dgn-np:NP61676.RAFVazj2MuKGZdfHzLvEY0oCmI44XqelEMngQMeh_gGZ0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP61676.RAFVazj2MuKGZdfHzLvEY0oCmI44XqelEMngQMeh_gGZ0130_assertion {
  miriam-gene:4846 a ncit:C16612 .
  
  lld:C0038454 a ncit:C7057 .
  
  dgn-gda:DGNf9cc49cdb62fb69cf0847f5db2486063 sio:SIO_000628 miriam-gene:4846, lld:C0038454;
    a sio:SIO_001122 .
}

dgn-np:NP61676.RAFVazj2MuKGZdfHzLvEY0oCmI44XqelEMngQMeh_gGZ0130_provenance {
  dgn-np:NP61676.RAFVazj2MuKGZdfHzLvEY0oCmI44XqelEMngQMeh_gGZ0130_assertion dcterms:description
      "[ Homozygosity for the G allele of the Glu298Asp polymorphism in NOS3 was associated with BI, and especially with lacunar stroke. Our findings suggest that genetic susceptibility and LDL cholesterol have a synergistic relation. Although these findings should be replicated in a larger sample of subjects and the functionality of the Glu298Asp polymorphism has not been established, these results may help us to understand the cause of the arteriolopathy underlying lacunae and have future implications in their treatment and prevention.]. 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:10884465;
    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:NP61676.RAFVazj2MuKGZdfHzLvEY0oCmI44XqelEMngQMeh_gGZ0130_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" .
}