@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP84544.RA-wu2oFLDVRZLgiNaHGgx1iMqx-1shHW4DL9NcRVCPyo> .
@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:NP84544.RA-wu2oFLDVRZLgiNaHGgx1iMqx-1shHW4DL9NcRVCPyo130_head {
  this: np:hasAssertion dgn-np:NP84544.RA-wu2oFLDVRZLgiNaHGgx1iMqx-1shHW4DL9NcRVCPyo130_assertion ;
    np:hasProvenance dgn-np:NP84544.RA-wu2oFLDVRZLgiNaHGgx1iMqx-1shHW4DL9NcRVCPyo130_provenance ;
    np:hasPublicationInfo dgn-np:NP84544.RA-wu2oFLDVRZLgiNaHGgx1iMqx-1shHW4DL9NcRVCPyo130_publicationInfo ;
    a np:Nanopublication .
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}
dgn-np:NP84544.RA-wu2oFLDVRZLgiNaHGgx1iMqx-1shHW4DL9NcRVCPyo130_assertion {
  miriam-gene:4038 a ncit:C16612 .
  lld:C0029456 a ncit:C7057 .
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    a sio:SIO_001122 .
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dgn-np:NP84544.RA-wu2oFLDVRZLgiNaHGgx1iMqx-1shHW4DL9NcRVCPyo130_provenance {
  dgn-np:NP84544.RA-wu2oFLDVRZLgiNaHGgx1iMqx-1shHW4DL9NcRVCPyo130_assertion dcterms: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 ;
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    prov:wasDerivedFrom dgn-void:gad-20130706 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
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  dgn-void:source_evidence_literature a eco:ECO_0000212 ;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
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}
dgn-np:NP84544.RA-wu2oFLDVRZLgiNaHGgx1iMqx-1shHW4DL9NcRVCPyo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:41+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
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