@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP87703.RAXNXWx1SmfIURiwOQrn2d2Fek56dG6to9TUwr-Y5G3cY> .
@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:NP87703.RAXNXWx1SmfIURiwOQrn2d2Fek56dG6to9TUwr-Y5G3cY130_head {
  this: np:hasAssertion dgn-np:NP87703.RAXNXWx1SmfIURiwOQrn2d2Fek56dG6to9TUwr-Y5G3cY130_assertion;
    np:hasProvenance dgn-np:NP87703.RAXNXWx1SmfIURiwOQrn2d2Fek56dG6to9TUwr-Y5G3cY130_provenance;
    np:hasPublicationInfo dgn-np:NP87703.RAXNXWx1SmfIURiwOQrn2d2Fek56dG6to9TUwr-Y5G3cY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP87703.RAXNXWx1SmfIURiwOQrn2d2Fek56dG6to9TUwr-Y5G3cY130_assertion a np:Assertion .
  
  dgn-np:NP87703.RAXNXWx1SmfIURiwOQrn2d2Fek56dG6to9TUwr-Y5G3cY130_provenance a np:Provenance .
  
  dgn-np:NP87703.RAXNXWx1SmfIURiwOQrn2d2Fek56dG6to9TUwr-Y5G3cY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP87703.RAXNXWx1SmfIURiwOQrn2d2Fek56dG6to9TUwr-Y5G3cY130_assertion {
  miriam-gene:2247 a ncit:C16612 .
  
  lld:C0029456 a ncit:C7057 .
  
  dgn-gda:DGNfd19853af474e8f6876886f780a439c1 sio:SIO_000628 miriam-gene:2247, lld:C0029456;
    a sio:SIO_001122 .
}

dgn-np:NP87703.RAXNXWx1SmfIURiwOQrn2d2Fek56dG6to9TUwr-Y5G3cY130_provenance {
  dgn-np:NP87703.RAXNXWx1SmfIURiwOQrn2d2Fek56dG6to9TUwr-Y5G3cY130_assertion dcterms:description
      "[Our initial and replicate association studies and subsequent gene expression analyses support the conclusion that these three polymorphisms of the FGF2 gene may contribute to susceptibility to osteoporosis, most likely through their effects on altered binding affinity for specific miRNAs.]. 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:20641033;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP87703.RAXNXWx1SmfIURiwOQrn2d2Fek56dG6to9TUwr-Y5G3cY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:43+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" .
}