@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP171822.RA5IrVc4xAZjnyqcclUtYeeKqIc4DYKdD_BRGsxFEf8rQ> .
@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:NP171822.RA5IrVc4xAZjnyqcclUtYeeKqIc4DYKdD_BRGsxFEf8rQ130_head {
  this: np:hasAssertion dgn-np:NP171822.RA5IrVc4xAZjnyqcclUtYeeKqIc4DYKdD_BRGsxFEf8rQ130_assertion ;
    np:hasProvenance dgn-np:NP171822.RA5IrVc4xAZjnyqcclUtYeeKqIc4DYKdD_BRGsxFEf8rQ130_provenance ;
    np:hasPublicationInfo dgn-np:NP171822.RA5IrVc4xAZjnyqcclUtYeeKqIc4DYKdD_BRGsxFEf8rQ130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP171822.RA5IrVc4xAZjnyqcclUtYeeKqIc4DYKdD_BRGsxFEf8rQ130_assertion a np:Assertion .
  dgn-np:NP171822.RA5IrVc4xAZjnyqcclUtYeeKqIc4DYKdD_BRGsxFEf8rQ130_provenance a np:Provenance .
  dgn-np:NP171822.RA5IrVc4xAZjnyqcclUtYeeKqIc4DYKdD_BRGsxFEf8rQ130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP171822.RA5IrVc4xAZjnyqcclUtYeeKqIc4DYKdD_BRGsxFEf8rQ130_assertion {
  miriam-gene:7439 a ncit:C16612 .
  lld:C2678504 a ncit:C7057 .
  dgn-gda:DGN3d36536814692d383fb03ae980a2340b sio:SIO_000628 miriam-gene:7439 , lld:C2678504 ;
    a sio:SIO_001121 .
}
dgn-np:NP171822.RA5IrVc4xAZjnyqcclUtYeeKqIc4DYKdD_BRGsxFEf8rQ130_provenance {
  dgn-np:NP171822.RA5IrVc4xAZjnyqcclUtYeeKqIc4DYKdD_BRGsxFEf8rQ130_assertion dcterms:description "[As variations in the TNFRSF11B gene could alter the susceptibility to osteoporosis, the aim of study was to investigate association of two TNFRSF11B gene polymorphisms with BMD and serum OPG concentration in postmenopausal women.]. 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:21411255 ;
    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:NP171822.RA5IrVc4xAZjnyqcclUtYeeKqIc4DYKdD_BRGsxFEf8rQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:33+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" .
}