@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP179172.RAbFcn0Jb28Vw9D_qy_G6GIrEjEHpCxl3bjmg5TbLo2GQ> .
@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:NP179172.RAbFcn0Jb28Vw9D_qy_G6GIrEjEHpCxl3bjmg5TbLo2GQ130_head {
  this: np:hasAssertion dgn-np:NP179172.RAbFcn0Jb28Vw9D_qy_G6GIrEjEHpCxl3bjmg5TbLo2GQ130_assertion ;
    np:hasProvenance dgn-np:NP179172.RAbFcn0Jb28Vw9D_qy_G6GIrEjEHpCxl3bjmg5TbLo2GQ130_provenance ;
    np:hasPublicationInfo dgn-np:NP179172.RAbFcn0Jb28Vw9D_qy_G6GIrEjEHpCxl3bjmg5TbLo2GQ130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP179172.RAbFcn0Jb28Vw9D_qy_G6GIrEjEHpCxl3bjmg5TbLo2GQ130_assertion a np:Assertion .
  dgn-np:NP179172.RAbFcn0Jb28Vw9D_qy_G6GIrEjEHpCxl3bjmg5TbLo2GQ130_provenance a np:Provenance .
  dgn-np:NP179172.RAbFcn0Jb28Vw9D_qy_G6GIrEjEHpCxl3bjmg5TbLo2GQ130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP179172.RAbFcn0Jb28Vw9D_qy_G6GIrEjEHpCxl3bjmg5TbLo2GQ130_assertion {
  miriam-gene:7439 a ncit:C16612 .
  lld:C2678504 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP179172.RAbFcn0Jb28Vw9D_qy_G6GIrEjEHpCxl3bjmg5TbLo2GQ130_provenance {
  dgn-np:NP179172.RAbFcn0Jb28Vw9D_qy_G6GIrEjEHpCxl3bjmg5TbLo2GQ130_assertion dcterms:description "[To evaluate whether common allelic variants in the gene encoding the vitamin D receptor (VDR) were useful in predicting differences in bone mineral density (BMD) and bone turnover rate in Koreans, we analyzed the restriction pattern of the polymerase chain reaction product of the VDR gene with the Bsm1 enzyme and serum osteocalcin in patients with osteoporosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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    prov:wasDerivedFrom dgn-void:befree-20140225 ;
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}
dgn-np:NP179172.RAbFcn0Jb28Vw9D_qy_G6GIrEjEHpCxl3bjmg5TbLo2GQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:37+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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}