@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP197282.RA8Pqt5Z2NC_7yvRberV_OQFit-xv15MilqbUkdl95D4g> .
@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:NP197282.RA8Pqt5Z2NC_7yvRberV_OQFit-xv15MilqbUkdl95D4g130_head {
  this: np:hasAssertion dgn-np:NP197282.RA8Pqt5Z2NC_7yvRberV_OQFit-xv15MilqbUkdl95D4g130_assertion;
    np:hasProvenance dgn-np:NP197282.RA8Pqt5Z2NC_7yvRberV_OQFit-xv15MilqbUkdl95D4g130_provenance;
    np:hasPublicationInfo dgn-np:NP197282.RA8Pqt5Z2NC_7yvRberV_OQFit-xv15MilqbUkdl95D4g130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP197282.RA8Pqt5Z2NC_7yvRberV_OQFit-xv15MilqbUkdl95D4g130_assertion a np:Assertion .
  
  dgn-np:NP197282.RA8Pqt5Z2NC_7yvRberV_OQFit-xv15MilqbUkdl95D4g130_provenance a np:Provenance .
  
  dgn-np:NP197282.RA8Pqt5Z2NC_7yvRberV_OQFit-xv15MilqbUkdl95D4g130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP197282.RA8Pqt5Z2NC_7yvRberV_OQFit-xv15MilqbUkdl95D4g130_assertion {
  miriam-gene:1756 a ncit:C16612 .
  
  lld:C2678504 a ncit:C7057 .
  
  dgn-gda:DGN4fe35f98d895f7b241d56c27295536e2 sio:SIO_000628 miriam-gene:1756, lld:C2678504;
    a sio:SIO_001121 .
}

dgn-np:NP197282.RA8Pqt5Z2NC_7yvRberV_OQFit-xv15MilqbUkdl95D4g130_provenance {
  dgn-np:NP197282.RA8Pqt5Z2NC_7yvRberV_OQFit-xv15MilqbUkdl95D4g130_assertion dcterms:description
      "[Osteoporosis is a systemic disorder of decreased skeletal mass as measured by bone mineral density (BMD), and disturbed skeletal architecture and function which results in an increased risk for bone fractures with consecutively increased morbidity and mortality.]. 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:10812458;
    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:NP197282.RA8Pqt5Z2NC_7yvRberV_OQFit-xv15MilqbUkdl95D4g130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:48+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" .
}