@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP466244.RAEiuLQgyESsaySejCOtUNowAyZa2FUeCG7C-tXg9Bui8> .
@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:NP466244.RAEiuLQgyESsaySejCOtUNowAyZa2FUeCG7C-tXg9Bui8130_head {
  this: np:hasAssertion dgn-np:NP466244.RAEiuLQgyESsaySejCOtUNowAyZa2FUeCG7C-tXg9Bui8130_assertion ;
    np:hasProvenance dgn-np:NP466244.RAEiuLQgyESsaySejCOtUNowAyZa2FUeCG7C-tXg9Bui8130_provenance ;
    np:hasPublicationInfo dgn-np:NP466244.RAEiuLQgyESsaySejCOtUNowAyZa2FUeCG7C-tXg9Bui8130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP466244.RAEiuLQgyESsaySejCOtUNowAyZa2FUeCG7C-tXg9Bui8130_assertion a np:Assertion .
  dgn-np:NP466244.RAEiuLQgyESsaySejCOtUNowAyZa2FUeCG7C-tXg9Bui8130_provenance a np:Provenance .
  dgn-np:NP466244.RAEiuLQgyESsaySejCOtUNowAyZa2FUeCG7C-tXg9Bui8130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP466244.RAEiuLQgyESsaySejCOtUNowAyZa2FUeCG7C-tXg9Bui8130_assertion {
  miriam-gene:7439 a ncit:C16612 .
  lld:C0432222 a ncit:C7057 .
  dgn-gda:DGN52befc00b307fa50471f397f4559fc96 sio:SIO_000628 miriam-gene:7439 , lld:C0432222 ;
    a sio:SIO_001121 .
}
dgn-np:NP466244.RAEiuLQgyESsaySejCOtUNowAyZa2FUeCG7C-tXg9Bui8130_provenance {
  dgn-np:NP466244.RAEiuLQgyESsaySejCOtUNowAyZa2FUeCG7C-tXg9Bui8130_assertion dcterms:description "[No significant association was observed between BMD values at the lumbar spine (LS) and femoral neck (FN) in relation to PvuII and XbaI polymorphisms individually, but haplotype analysis showed that BMD values (Z score) were significantly lower in those who carried the Px haplotype (n = 36) compared with those who did not (n = 170) at both the LS (mean +/- SEM; -0.775 +/- 0.125 vs. -0.285 +/- 0.082;p = 0.002) and the FN (-0.888 +/- 0.130 vs. -0.335 +/- 0.083; p = 0.0006).]. 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:11149476 ;
    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:NP466244.RAEiuLQgyESsaySejCOtUNowAyZa2FUeCG7C-tXg9Bui8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:39+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" .
}