@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP641301.RACnf0Y11nWY8vFL_CeZYgdlsw3V2XLpJoOs2P1ZViaxE> .
@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:NP641301.RACnf0Y11nWY8vFL_CeZYgdlsw3V2XLpJoOs2P1ZViaxE130_head {
  this: np:hasAssertion dgn-np:NP641301.RACnf0Y11nWY8vFL_CeZYgdlsw3V2XLpJoOs2P1ZViaxE130_assertion;
    np:hasProvenance dgn-np:NP641301.RACnf0Y11nWY8vFL_CeZYgdlsw3V2XLpJoOs2P1ZViaxE130_provenance;
    np:hasPublicationInfo dgn-np:NP641301.RACnf0Y11nWY8vFL_CeZYgdlsw3V2XLpJoOs2P1ZViaxE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP641301.RACnf0Y11nWY8vFL_CeZYgdlsw3V2XLpJoOs2P1ZViaxE130_assertion a np:Assertion .
  
  dgn-np:NP641301.RACnf0Y11nWY8vFL_CeZYgdlsw3V2XLpJoOs2P1ZViaxE130_provenance a np:Provenance .
  
  dgn-np:NP641301.RACnf0Y11nWY8vFL_CeZYgdlsw3V2XLpJoOs2P1ZViaxE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP641301.RACnf0Y11nWY8vFL_CeZYgdlsw3V2XLpJoOs2P1ZViaxE130_assertion {
  miriam-gene:1535 a ncit:C16612 .
  
  lld:C0520679 a ncit:C7057 .
  
  dgn-gda:DGNec1bca83100f5c2837a77dbe9b49227a sio:SIO_000628 miriam-gene:1535, lld:C0520679;
    a sio:SIO_001121 .
}

dgn-np:NP641301.RACnf0Y11nWY8vFL_CeZYgdlsw3V2XLpJoOs2P1ZViaxE130_provenance {
  dgn-np:NP641301.RACnf0Y11nWY8vFL_CeZYgdlsw3V2XLpJoOs2P1ZViaxE130_assertion dcterms:description
      "[The frequencies of NADPH oxidase (NOX) polymorphisms in the p22phox subunit were similar between children with OSA and controls, except for rs6520785 and rs4673, the latter being significantly more frequent among the OSA children without deficits than with deficits (p<0.02).]. 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:21902598;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP641301.RACnf0Y11nWY8vFL_CeZYgdlsw3V2XLpJoOs2P1ZViaxE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:26+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" .
}