@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP44788.RAnCsRpZS-_tSYiS5QMZyjIXzeqXgR5CfO21x1BFLc9ho> .
@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:NP44788.RAnCsRpZS-_tSYiS5QMZyjIXzeqXgR5CfO21x1BFLc9ho130_head {
  this: np:hasAssertion dgn-np:NP44788.RAnCsRpZS-_tSYiS5QMZyjIXzeqXgR5CfO21x1BFLc9ho130_assertion;
    np:hasProvenance dgn-np:NP44788.RAnCsRpZS-_tSYiS5QMZyjIXzeqXgR5CfO21x1BFLc9ho130_provenance;
    np:hasPublicationInfo dgn-np:NP44788.RAnCsRpZS-_tSYiS5QMZyjIXzeqXgR5CfO21x1BFLc9ho130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP44788.RAnCsRpZS-_tSYiS5QMZyjIXzeqXgR5CfO21x1BFLc9ho130_assertion a np:Assertion .
  
  dgn-np:NP44788.RAnCsRpZS-_tSYiS5QMZyjIXzeqXgR5CfO21x1BFLc9ho130_provenance a np:Provenance .
  
  dgn-np:NP44788.RAnCsRpZS-_tSYiS5QMZyjIXzeqXgR5CfO21x1BFLc9ho130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP44788.RAnCsRpZS-_tSYiS5QMZyjIXzeqXgR5CfO21x1BFLc9ho130_assertion {
  miriam-gene:2099 a ncit:C16612 .
  
  lld:C0428796 a ncit:C7057 .
  
  dgn-gda:DGN87177849015c3c38d715da0d5a713b17 sio:SIO_000628 miriam-gene:2099, lld:C0428796;
    a sio:SIO_001122 .
}

dgn-np:NP44788.RAnCsRpZS-_tSYiS5QMZyjIXzeqXgR5CfO21x1BFLc9ho130_provenance {
  dgn-np:NP44788.RAnCsRpZS-_tSYiS5QMZyjIXzeqXgR5CfO21x1BFLc9ho130_assertion dct:description
      "[ We have demonstrated that the PvuII polymorphism in the ORalpha gene is related to both the presence of AS in postmenopausal women and to lipid levels in adolescent females, suggesting that this polymorphism may influence the risk of AS partly by affecting lipid levels.]. 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:12859695;
    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:NP44788.RAnCsRpZS-_tSYiS5QMZyjIXzeqXgR5CfO21x1BFLc9ho130_publicationInfo {
  this: dct:created "2014-10-02T12:32:20+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" .
}