@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP57574.RAaazz-WFYZTlt412Y5uMCaZd9FmOQDr_g4PcVpWhFK5U> .
@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:NP57574.RAaazz-WFYZTlt412Y5uMCaZd9FmOQDr_g4PcVpWhFK5U130_head {
  this: np:hasAssertion dgn-np:NP57574.RAaazz-WFYZTlt412Y5uMCaZd9FmOQDr_g4PcVpWhFK5U130_assertion;
    np:hasProvenance dgn-np:NP57574.RAaazz-WFYZTlt412Y5uMCaZd9FmOQDr_g4PcVpWhFK5U130_provenance;
    np:hasPublicationInfo dgn-np:NP57574.RAaazz-WFYZTlt412Y5uMCaZd9FmOQDr_g4PcVpWhFK5U130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP57574.RAaazz-WFYZTlt412Y5uMCaZd9FmOQDr_g4PcVpWhFK5U130_assertion a np:Assertion .
  
  dgn-np:NP57574.RAaazz-WFYZTlt412Y5uMCaZd9FmOQDr_g4PcVpWhFK5U130_provenance a np:Provenance .
  
  dgn-np:NP57574.RAaazz-WFYZTlt412Y5uMCaZd9FmOQDr_g4PcVpWhFK5U130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP57574.RAaazz-WFYZTlt412Y5uMCaZd9FmOQDr_g4PcVpWhFK5U130_assertion {
  miriam-gene:3240 a ncit:C16612 .
  
  lld:C0007222 a ncit:C7057 .
  
  dgn-gda:DGN78c0dcd5ca50dc7eb9be50235bdd73ab sio:SIO_000628 miriam-gene:3240, lld:C0007222;
    a sio:SIO_001122 .
}

dgn-np:NP57574.RAaazz-WFYZTlt412Y5uMCaZd9FmOQDr_g4PcVpWhFK5U130_provenance {
  dgn-np:NP57574.RAaazz-WFYZTlt412Y5uMCaZd9FmOQDr_g4PcVpWhFK5U130_assertion dcterms:description
      "[These results suggest that haptoglobin phenotype is an important risk factor in determining susceptibility to cardiovascular disease in obstructive sleep apnea syndrome, which may be mediated by the decreased antioxidant and antiinflammatory actions of the haptoglobin 2 allelic protein product.]. 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:12938813;
    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:NP57574.RAaazz-WFYZTlt412Y5uMCaZd9FmOQDr_g4PcVpWhFK5U130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:27+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" .
}