@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP338933.RAmHkvzSN3fmbtNRcX_n0CdnXdU7y3tBLnjOFPAR7VZVA> .
@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:NP338933.RAmHkvzSN3fmbtNRcX_n0CdnXdU7y3tBLnjOFPAR7VZVA130_head {
  this: np:hasAssertion dgn-np:NP338933.RAmHkvzSN3fmbtNRcX_n0CdnXdU7y3tBLnjOFPAR7VZVA130_assertion;
    np:hasProvenance dgn-np:NP338933.RAmHkvzSN3fmbtNRcX_n0CdnXdU7y3tBLnjOFPAR7VZVA130_provenance;
    np:hasPublicationInfo dgn-np:NP338933.RAmHkvzSN3fmbtNRcX_n0CdnXdU7y3tBLnjOFPAR7VZVA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP338933.RAmHkvzSN3fmbtNRcX_n0CdnXdU7y3tBLnjOFPAR7VZVA130_assertion a np:Assertion .
  
  dgn-np:NP338933.RAmHkvzSN3fmbtNRcX_n0CdnXdU7y3tBLnjOFPAR7VZVA130_provenance a np:Provenance .
  
  dgn-np:NP338933.RAmHkvzSN3fmbtNRcX_n0CdnXdU7y3tBLnjOFPAR7VZVA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP338933.RAmHkvzSN3fmbtNRcX_n0CdnXdU7y3tBLnjOFPAR7VZVA130_assertion {
  miriam-gene:4982 a ncit:C16612 .
  
  lld:C0521170 a ncit:C7057 .
  
  dgn-gda:DGNfdccf66109e53e593491c55bd794ad9f sio:SIO_000628 miriam-gene:4982, lld:C0521170;
    a sio:SIO_001121 .
}

dgn-np:NP338933.RAmHkvzSN3fmbtNRcX_n0CdnXdU7y3tBLnjOFPAR7VZVA130_provenance {
  dgn-np:NP338933.RAmHkvzSN3fmbtNRcX_n0CdnXdU7y3tBLnjOFPAR7VZVA130_assertion dcterms:description
      "[We investigated the association between a Lys3Asn polymorphism in the OPG gene and bone mineral density (BMD), and the risk of fracture in 6695 women aged 65 yr and older participating in the Study of Osteoporotic Fractures.]. 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:18319311;
    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:NP338933.RAmHkvzSN3fmbtNRcX_n0CdnXdU7y3tBLnjOFPAR7VZVA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:19+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" .
}