@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP79484.RA5AfDN8ADz18Bfy-RJtxW-7T7UaRAPBBt46UM5fvVh_o> .
@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:NP79484.RA5AfDN8ADz18Bfy-RJtxW-7T7UaRAPBBt46UM5fvVh_o130_head {
  this: np:hasAssertion dgn-np:NP79484.RA5AfDN8ADz18Bfy-RJtxW-7T7UaRAPBBt46UM5fvVh_o130_assertion;
    np:hasProvenance dgn-np:NP79484.RA5AfDN8ADz18Bfy-RJtxW-7T7UaRAPBBt46UM5fvVh_o130_provenance;
    np:hasPublicationInfo dgn-np:NP79484.RA5AfDN8ADz18Bfy-RJtxW-7T7UaRAPBBt46UM5fvVh_o130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP79484.RA5AfDN8ADz18Bfy-RJtxW-7T7UaRAPBBt46UM5fvVh_o130_assertion a np:Assertion .
  
  dgn-np:NP79484.RA5AfDN8ADz18Bfy-RJtxW-7T7UaRAPBBt46UM5fvVh_o130_provenance a np:Provenance .
  
  dgn-np:NP79484.RA5AfDN8ADz18Bfy-RJtxW-7T7UaRAPBBt46UM5fvVh_o130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP79484.RA5AfDN8ADz18Bfy-RJtxW-7T7UaRAPBBt46UM5fvVh_o130_assertion {
  miriam-gene:767 a ncit:C16612 .
  
  lld:C0029456 a ncit:C7057 .
  
  dgn-gda:DGNd0c569fdee10f53675023583da0d9dc1 sio:SIO_000628 miriam-gene:767, lld:C0029456;
    a sio:SIO_001122 .
}

dgn-np:NP79484.RA5AfDN8ADz18Bfy-RJtxW-7T7UaRAPBBt46UM5fvVh_o130_provenance {
  dgn-np:NP79484.RA5AfDN8ADz18Bfy-RJtxW-7T7UaRAPBBt46UM5fvVh_o130_assertion dct:description
      "[Here, we investigated single nucleotide polymorphisms (SNPs) in carbonic anhydrase genes that are expressed in bone tissues, i.e., CA8 and CA10, for possible association with femoral and lumbar BMD among 337 Japanese women with osteoporosis participated in BioBank Japan project.]. 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:19172221;
    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:NP79484.RA5AfDN8ADz18Bfy-RJtxW-7T7UaRAPBBt46UM5fvVh_o130_publicationInfo {
  this: dct:created "2014-10-02T12:32:39+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}