@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP780745.RA19rTEY23KfA-HLoX_aR7z9-YyxTGxO6icF5p6uwX-Ig> .
@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:NP780745.RA19rTEY23KfA-HLoX_aR7z9-YyxTGxO6icF5p6uwX-Ig130_head {
  this: np:hasAssertion dgn-np:NP780745.RA19rTEY23KfA-HLoX_aR7z9-YyxTGxO6icF5p6uwX-Ig130_assertion;
    np:hasProvenance dgn-np:NP780745.RA19rTEY23KfA-HLoX_aR7z9-YyxTGxO6icF5p6uwX-Ig130_provenance;
    np:hasPublicationInfo dgn-np:NP780745.RA19rTEY23KfA-HLoX_aR7z9-YyxTGxO6icF5p6uwX-Ig130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP780745.RA19rTEY23KfA-HLoX_aR7z9-YyxTGxO6icF5p6uwX-Ig130_assertion a np:Assertion .
  
  dgn-np:NP780745.RA19rTEY23KfA-HLoX_aR7z9-YyxTGxO6icF5p6uwX-Ig130_provenance a np:Provenance .
  
  dgn-np:NP780745.RA19rTEY23KfA-HLoX_aR7z9-YyxTGxO6icF5p6uwX-Ig130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP780745.RA19rTEY23KfA-HLoX_aR7z9-YyxTGxO6icF5p6uwX-Ig130_assertion {
  miriam-gene:860 a ncit:C16612 .
  
  lld:C2678504 a ncit:C7057 .
  
  dgn-gda:DGN9ba6ea930074ecd4ec7fa0b7668557d9 sio:SIO_000628 miriam-gene:860, lld:C2678504;
    a sio:SIO_001121 .
}

dgn-np:NP780745.RA19rTEY23KfA-HLoX_aR7z9-YyxTGxO6icF5p6uwX-Ig130_provenance {
  dgn-np:NP780745.RA19rTEY23KfA-HLoX_aR7z9-YyxTGxO6icF5p6uwX-Ig130_assertion dcterms:description
      "[enhanced mRNA expression of known osteoporosis-associated genes (LRP5, RUNX2, COL1A1) and of genes involved in osteoclastogenesis (CSF1, PTH1R), but most notably of genes coding for inhibitors of WNT and BMP signaling, such as Sclerostin and MAB21L2.]. 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:23028809;
    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:NP780745.RA19rTEY23KfA-HLoX_aR7z9-YyxTGxO6icF5p6uwX-Ig130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:53+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" .
}