@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP396454.RAD_CkllXNbXW_8qpgT03sMnEFXV1nnFkeDs8cr8PjJWs> .
@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:NP396454.RAD_CkllXNbXW_8qpgT03sMnEFXV1nnFkeDs8cr8PjJWs130_head {
  this: np:hasAssertion dgn-np:NP396454.RAD_CkllXNbXW_8qpgT03sMnEFXV1nnFkeDs8cr8PjJWs130_assertion;
    np:hasProvenance dgn-np:NP396454.RAD_CkllXNbXW_8qpgT03sMnEFXV1nnFkeDs8cr8PjJWs130_provenance;
    np:hasPublicationInfo dgn-np:NP396454.RAD_CkllXNbXW_8qpgT03sMnEFXV1nnFkeDs8cr8PjJWs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP396454.RAD_CkllXNbXW_8qpgT03sMnEFXV1nnFkeDs8cr8PjJWs130_assertion a np:Assertion .
  
  dgn-np:NP396454.RAD_CkllXNbXW_8qpgT03sMnEFXV1nnFkeDs8cr8PjJWs130_provenance a np:Provenance .
  
  dgn-np:NP396454.RAD_CkllXNbXW_8qpgT03sMnEFXV1nnFkeDs8cr8PjJWs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP396454.RAD_CkllXNbXW_8qpgT03sMnEFXV1nnFkeDs8cr8PjJWs130_assertion {
  miriam-gene:1234 a ncit:C16612 .
  
  lld:C0011881 a ncit:C7057 .
  
  dgn-gda:DGN2aacafdf3533e4fda3fa44bef1a310e0 sio:SIO_000628 miriam-gene:1234, lld:C0011881;
    a sio:SIO_001121 .
}

dgn-np:NP396454.RAD_CkllXNbXW_8qpgT03sMnEFXV1nnFkeDs8cr8PjJWs130_provenance {
  dgn-np:NP396454.RAD_CkllXNbXW_8qpgT03sMnEFXV1nnFkeDs8cr8PjJWs130_assertion dcterms:description
      "[Male carriers of the 59029G allele, which is associated with diminished expression of CCR5 on the surface of immunocompetent cells, had significantly higher risk of developing diabetic nephropathy than noncarriers (OR [95% CI] 1.9 [1.2-3.0]).]. 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:16249462;
    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:NP396454.RAD_CkllXNbXW_8qpgT03sMnEFXV1nnFkeDs8cr8PjJWs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:56+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" .
}