@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP391349.RAjVlhFvNrG1FxKrl6MGiblFzgw381ee8A_YMy2UaLN4k> .
@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:NP391349.RAjVlhFvNrG1FxKrl6MGiblFzgw381ee8A_YMy2UaLN4k130_head {
  this: np:hasAssertion dgn-np:NP391349.RAjVlhFvNrG1FxKrl6MGiblFzgw381ee8A_YMy2UaLN4k130_assertion;
    np:hasProvenance dgn-np:NP391349.RAjVlhFvNrG1FxKrl6MGiblFzgw381ee8A_YMy2UaLN4k130_provenance;
    np:hasPublicationInfo dgn-np:NP391349.RAjVlhFvNrG1FxKrl6MGiblFzgw381ee8A_YMy2UaLN4k130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP391349.RAjVlhFvNrG1FxKrl6MGiblFzgw381ee8A_YMy2UaLN4k130_assertion a np:Assertion .
  
  dgn-np:NP391349.RAjVlhFvNrG1FxKrl6MGiblFzgw381ee8A_YMy2UaLN4k130_provenance a np:Provenance .
  
  dgn-np:NP391349.RAjVlhFvNrG1FxKrl6MGiblFzgw381ee8A_YMy2UaLN4k130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP391349.RAjVlhFvNrG1FxKrl6MGiblFzgw381ee8A_YMy2UaLN4k130_assertion {
  miriam-gene:5669 a ncit:C16612 .
  
  lld:C0008312 a ncit:C7057 .
  
  dgn-gda:DGN69b38b9f519855b7fd8c444617718ed7 sio:SIO_000628 miriam-gene:5669, lld:C0008312;
    a sio:SIO_001121 .
}

dgn-np:NP391349.RAjVlhFvNrG1FxKrl6MGiblFzgw381ee8A_YMy2UaLN4k130_provenance {
  dgn-np:NP391349.RAjVlhFvNrG1FxKrl6MGiblFzgw381ee8A_YMy2UaLN4k130_assertion dcterms:description
      "[The potential influence of two gene polymorphisms, vitamin D receptor gene (VDR) and the gene encoding collagen type Ialpha1 (COLIA1) Sp1 polymorphisms, in the reduced bone mass observed in patients with primary biliary cirrhosis (PBC) was assessed in 61 women with PBC (age, 54.1 +/- 1.1 years) by restriction enzyme digestion of polymerase chain reaction (PCR)-amplified DNA extracted from whole blood.]. 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:11230734;
    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:NP391349.RAjVlhFvNrG1FxKrl6MGiblFzgw381ee8A_YMy2UaLN4k130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:53+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" .
}