@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP254322.RAWp9FvlPj4mfQjorVKDUqEEwEpvW-WDUkEmA8_htxq-Q> .
@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:NP254322.RAWp9FvlPj4mfQjorVKDUqEEwEpvW-WDUkEmA8_htxq-Q130_head {
  this: np:hasAssertion dgn-np:NP254322.RAWp9FvlPj4mfQjorVKDUqEEwEpvW-WDUkEmA8_htxq-Q130_assertion;
    np:hasProvenance dgn-np:NP254322.RAWp9FvlPj4mfQjorVKDUqEEwEpvW-WDUkEmA8_htxq-Q130_provenance;
    np:hasPublicationInfo dgn-np:NP254322.RAWp9FvlPj4mfQjorVKDUqEEwEpvW-WDUkEmA8_htxq-Q130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP254322.RAWp9FvlPj4mfQjorVKDUqEEwEpvW-WDUkEmA8_htxq-Q130_assertion a np:Assertion .
  
  dgn-np:NP254322.RAWp9FvlPj4mfQjorVKDUqEEwEpvW-WDUkEmA8_htxq-Q130_provenance a np:Provenance .
  
  dgn-np:NP254322.RAWp9FvlPj4mfQjorVKDUqEEwEpvW-WDUkEmA8_htxq-Q130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP254322.RAWp9FvlPj4mfQjorVKDUqEEwEpvW-WDUkEmA8_htxq-Q130_assertion {
  miriam-gene:199699 a ncit:C16612 .
  
  lld:C0521170 a ncit:C7057 .
  
  dgn-gda:DGNdfd64d931a30d71dfbb63cdf599aa373 sio:SIO_000628 miriam-gene:199699, lld:C0521170;
    a sio:SIO_001121 .
}

dgn-np:NP254322.RAWp9FvlPj4mfQjorVKDUqEEwEpvW-WDUkEmA8_htxq-Q130_provenance {
  dgn-np:NP254322.RAWp9FvlPj4mfQjorVKDUqEEwEpvW-WDUkEmA8_htxq-Q130_assertion dcterms:description
      "[Therefore our study may provide evidence that the Sp1 polymorphism may ameliorate the effects of HRT on BMD, suggesting some additional regimens may be used to support bone strength and to decrease 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:18226133;
    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:NP254322.RAWp9FvlPj4mfQjorVKDUqEEwEpvW-WDUkEmA8_htxq-Q130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:22+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" .
}