@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP799866.RAgM6tlTYSnf00__p61csfwr7Yw_MTEQMUvGJikZGHo8U> .
@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:NP799866.RAgM6tlTYSnf00__p61csfwr7Yw_MTEQMUvGJikZGHo8U130_head {
  this: np:hasAssertion dgn-np:NP799866.RAgM6tlTYSnf00__p61csfwr7Yw_MTEQMUvGJikZGHo8U130_assertion;
    np:hasProvenance dgn-np:NP799866.RAgM6tlTYSnf00__p61csfwr7Yw_MTEQMUvGJikZGHo8U130_provenance;
    np:hasPublicationInfo dgn-np:NP799866.RAgM6tlTYSnf00__p61csfwr7Yw_MTEQMUvGJikZGHo8U130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP799866.RAgM6tlTYSnf00__p61csfwr7Yw_MTEQMUvGJikZGHo8U130_assertion a np:Assertion .
  
  dgn-np:NP799866.RAgM6tlTYSnf00__p61csfwr7Yw_MTEQMUvGJikZGHo8U130_provenance a np:Provenance .
  
  dgn-np:NP799866.RAgM6tlTYSnf00__p61csfwr7Yw_MTEQMUvGJikZGHo8U130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP799866.RAgM6tlTYSnf00__p61csfwr7Yw_MTEQMUvGJikZGHo8U130_assertion {
  miriam-gene:7421 a ncit:C16612 .
  
  lld:C0022661 a ncit:C7057 .
  
  dgn-gda:DGN302d4e4a155327667e26ee8ec82a8ae4 sio:SIO_000628 miriam-gene:7421, lld:C0022661;
    a sio:SIO_001121 .
}

dgn-np:NP799866.RAgM6tlTYSnf00__p61csfwr7Yw_MTEQMUvGJikZGHo8U130_provenance {
  dgn-np:NP799866.RAgM6tlTYSnf00__p61csfwr7Yw_MTEQMUvGJikZGHo8U130_assertion dcterms:description
      "[No significant differences were observed in genotype or allele frequencies between case and control groups for VDR, CYP27B1 or CYP2R1 SNPs, either before or after stratification by recruitment centre or when restricted to patients with end-stage renal disease.]. 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:19783860;
    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:NP799866.RAgM6tlTYSnf00__p61csfwr7Yw_MTEQMUvGJikZGHo8U130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:11+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" .
}