@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP46319.RAg2xx-JvXGcOu3EprfjDt-uyYr_RY3SAceUl7rRnCDKY> .
@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 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:NP46319.RAg2xx-JvXGcOu3EprfjDt-uyYr_RY3SAceUl7rRnCDKY130_head {
   this: np:hasAssertion dgn-np:NP46319.RAg2xx-JvXGcOu3EprfjDt-uyYr_RY3SAceUl7rRnCDKY130_assertion ;
    np:hasProvenance dgn-np:NP46319.RAg2xx-JvXGcOu3EprfjDt-uyYr_RY3SAceUl7rRnCDKY130_provenance ;
    np:hasPublicationInfo dgn-np:NP46319.RAg2xx-JvXGcOu3EprfjDt-uyYr_RY3SAceUl7rRnCDKY130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP46319.RAg2xx-JvXGcOu3EprfjDt-uyYr_RY3SAceUl7rRnCDKY130_assertion a np:Assertion .
  dgn-np:NP46319.RAg2xx-JvXGcOu3EprfjDt-uyYr_RY3SAceUl7rRnCDKY130_provenance a np:Provenance .
  dgn-np:NP46319.RAg2xx-JvXGcOu3EprfjDt-uyYr_RY3SAceUl7rRnCDKY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP46319.RAg2xx-JvXGcOu3EprfjDt-uyYr_RY3SAceUl7rRnCDKY130_assertion {
   miriam-gene:1535 a ncit:C16612 .
  lld:C0010054 a ncit:C7057 .
  dgn-gda:DGN70dd54970b49c7cc7e61b39cba2cb520 sio:SIO_000628 miriam-gene:1535 , lld:C0010054 ;
    a sio:SIO_001122 .
}
dgn-np:NP46319.RAg2xx-JvXGcOu3EprfjDt-uyYr_RY3SAceUl7rRnCDKY130_provenance {
   dgn-np:NP46319.RAg2xx-JvXGcOu3EprfjDt-uyYr_RY3SAceUl7rRnCDKY130_assertion dct:description "[However, studies on the association of the C242T polymorphism in the p22phox gene with CAD have produced conflicting results, and the relation of this polymorphism with CAD is not well known in a population with acquired risk factors enhancing the NADPH-dependent superoxide production.]. 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:16923427 ;
    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:NP46319.RAg2xx-JvXGcOu3EprfjDt-uyYr_RY3SAceUl7rRnCDKY130_publicationInfo {
   this: dct:created "2014-10-02T12:32:21+02:00"^^xsd:dateTime ;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dct:rightsHolder dgn-void:IBIGroup ;
    dct:subject sio:SIO_000983 ;
    prv:usedData dgn-void:disgenetrdf ;
    pav:authoredBy orcid:0000-0001-5999-6269 , orcid:0000-0002-7534-7661 , orcid:0000-0002-9383-528X , orcid:0000-0003-0169-8159 , orcid:0000-0003-1244-7654 ;
    pav:createdBy orcid:0000-0003-0169-8159 ;
    pav:version "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}