@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP159303.RA9ualkyts97UowoINm6xgC2VLl-58bwXIFN94QH_DL7o> .
@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:NP159303.RA9ualkyts97UowoINm6xgC2VLl-58bwXIFN94QH_DL7o130_head {
  this: np:hasAssertion dgn-np:NP159303.RA9ualkyts97UowoINm6xgC2VLl-58bwXIFN94QH_DL7o130_assertion;
    np:hasProvenance dgn-np:NP159303.RA9ualkyts97UowoINm6xgC2VLl-58bwXIFN94QH_DL7o130_provenance;
    np:hasPublicationInfo dgn-np:NP159303.RA9ualkyts97UowoINm6xgC2VLl-58bwXIFN94QH_DL7o130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP159303.RA9ualkyts97UowoINm6xgC2VLl-58bwXIFN94QH_DL7o130_assertion a np:Assertion .
  
  dgn-np:NP159303.RA9ualkyts97UowoINm6xgC2VLl-58bwXIFN94QH_DL7o130_provenance a np:Provenance .
  
  dgn-np:NP159303.RA9ualkyts97UowoINm6xgC2VLl-58bwXIFN94QH_DL7o130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP159303.RA9ualkyts97UowoINm6xgC2VLl-58bwXIFN94QH_DL7o130_assertion {
  miriam-gene:1756 a ncit:C16612 .
  
  lld:C2678504 a ncit:C7057 .
  
  dgn-gda:DGN670f3b345e2a8b5c93ac801946a48fc4 sio:SIO_000628 miriam-gene:1756, lld:C2678504;
    a sio:SIO_001121 .
}

dgn-np:NP159303.RA9ualkyts97UowoINm6xgC2VLl-58bwXIFN94QH_DL7o130_provenance {
  dgn-np:NP159303.RA9ualkyts97UowoINm6xgC2VLl-58bwXIFN94QH_DL7o130_assertion dcterms:description
      "[This study suggests POSTN as a candidate gene for bone mineral density (BMD) variation and vertebral fracture risk, which could better our understanding about the genetic pathogenesis of osteoporosis and will be useful in clinic in the future.]. 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:22215184;
    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:NP159303.RA9ualkyts97UowoINm6xgC2VLl-58bwXIFN94QH_DL7o130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:26+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" .
}