@prefix dc: <http://purl.org/dc/terms/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP79495.RAWLw4tSdBGEvXzO_hpiiJX2Ape2DKLPy9GLx0vZecWHE> .
@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 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:NP79495.RAWLw4tSdBGEvXzO_hpiiJX2Ape2DKLPy9GLx0vZecWHE130_head {
  this: np:hasAssertion dgn-np:NP79495.RAWLw4tSdBGEvXzO_hpiiJX2Ape2DKLPy9GLx0vZecWHE130_assertion ;
    np:hasProvenance dgn-np:NP79495.RAWLw4tSdBGEvXzO_hpiiJX2Ape2DKLPy9GLx0vZecWHE130_provenance ;
    np:hasPublicationInfo dgn-np:NP79495.RAWLw4tSdBGEvXzO_hpiiJX2Ape2DKLPy9GLx0vZecWHE130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP79495.RAWLw4tSdBGEvXzO_hpiiJX2Ape2DKLPy9GLx0vZecWHE130_assertion a np:Assertion .
  dgn-np:NP79495.RAWLw4tSdBGEvXzO_hpiiJX2Ape2DKLPy9GLx0vZecWHE130_provenance a np:Provenance .
  dgn-np:NP79495.RAWLw4tSdBGEvXzO_hpiiJX2Ape2DKLPy9GLx0vZecWHE130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP79495.RAWLw4tSdBGEvXzO_hpiiJX2Ape2DKLPy9GLx0vZecWHE130_assertion {
  miriam-gene:50964 a ncit:C16612 .
  lld:C0029456 a ncit:C7057 .
  dgn-gda:DGNe7db8b43960242d7cc615dc2ea7a1d82 sio:SIO_000628 miriam-gene:50964 , lld:C0029456 ;
    a sio:SIO_001122 .
}
dgn-np:NP79495.RAWLw4tSdBGEvXzO_hpiiJX2Ape2DKLPy9GLx0vZecWHE130_provenance {
  dgn-np:NP79495.RAWLw4tSdBGEvXzO_hpiiJX2Ape2DKLPy9GLx0vZecWHE130_assertion dc:description "[Our study provides an independent replication of the associations between several SNPs in ZBTB40, ESR1, OPG, RANK, LRP5, and SOST with lumbar spine and/or total hip BMDs in a large sample of Han Chinese women. The results of this study further support the significant associations found between osteoporotic fracture and SNPs in SPTBN1 and SOST. Our results suggest that these variants represent osteoporosis susceptibility genes in both Han Chinese and European populations.]. 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:20554715 ;
    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:NP79495.RAWLw4tSdBGEvXzO_hpiiJX2Ape2DKLPy9GLx0vZecWHE130_publicationInfo {
  this: dc:created "2014-10-02T12:32:39+02:00"^^xsd:dateTime ;
    dc:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dc:rightsHolder dgn-void:IBIGroup ;
    dc: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" .
}