@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP51466.RA5KB_cr09VJ8gOzAjHpXi-0Pqh0gGE-JstCkVCtrWbmk> .
@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:NP51466.RA5KB_cr09VJ8gOzAjHpXi-0Pqh0gGE-JstCkVCtrWbmk130_head {
  this: np:hasAssertion dgn-np:NP51466.RA5KB_cr09VJ8gOzAjHpXi-0Pqh0gGE-JstCkVCtrWbmk130_assertion;
    np:hasProvenance dgn-np:NP51466.RA5KB_cr09VJ8gOzAjHpXi-0Pqh0gGE-JstCkVCtrWbmk130_provenance;
    np:hasPublicationInfo dgn-np:NP51466.RA5KB_cr09VJ8gOzAjHpXi-0Pqh0gGE-JstCkVCtrWbmk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP51466.RA5KB_cr09VJ8gOzAjHpXi-0Pqh0gGE-JstCkVCtrWbmk130_assertion a np:Assertion .
  
  dgn-np:NP51466.RA5KB_cr09VJ8gOzAjHpXi-0Pqh0gGE-JstCkVCtrWbmk130_provenance a np:Provenance .
  
  dgn-np:NP51466.RA5KB_cr09VJ8gOzAjHpXi-0Pqh0gGE-JstCkVCtrWbmk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP51466.RA5KB_cr09VJ8gOzAjHpXi-0Pqh0gGE-JstCkVCtrWbmk130_assertion {
  miriam-gene:6532 a ncit:C16612 .
  
  lld:C0851578 a ncit:C7057 .
  
  dgn-gda:DGNefa31f52cfb3bbbbc30096b5a1f2f45f sio:SIO_000628 miriam-gene:6532, lld:C0851578;
    a sio:SIO_001122 .
}

dgn-np:NP51466.RA5KB_cr09VJ8gOzAjHpXi-0Pqh0gGE-JstCkVCtrWbmk130_provenance {
  dgn-np:NP51466.RA5KB_cr09VJ8gOzAjHpXi-0Pqh0gGE-JstCkVCtrWbmk130_assertion dcterms:description
      "[ STG polymorphism appears to be associated with the occurrence of OSAS, especially in male patients. Absence of association of between genetic variants and polysomnography findings may suggest that some mechanisms other than STG polymorphism are involved in OSAS pathophysiology. Our results need confirmation in a larger group of patients with OSAS.]. 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:15867649;
    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:NP51466.RA5KB_cr09VJ8gOzAjHpXi-0Pqh0gGE-JstCkVCtrWbmk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:24+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" .
}