@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP77644.RAgCHEFNjEAJx3q3YuIuLie7BIDi2oGuNtvnwpDcGxF8M> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP77644.RAgCHEFNjEAJx3q3YuIuLie7BIDi2oGuNtvnwpDcGxF8M130_head {
  this: np:hasAssertion dgn-np:NP77644.RAgCHEFNjEAJx3q3YuIuLie7BIDi2oGuNtvnwpDcGxF8M130_assertion;
    np:hasProvenance dgn-np:NP77644.RAgCHEFNjEAJx3q3YuIuLie7BIDi2oGuNtvnwpDcGxF8M130_provenance;
    np:hasPublicationInfo dgn-np:NP77644.RAgCHEFNjEAJx3q3YuIuLie7BIDi2oGuNtvnwpDcGxF8M130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP77644.RAgCHEFNjEAJx3q3YuIuLie7BIDi2oGuNtvnwpDcGxF8M130_assertion a np:Assertion .
  
  dgn-np:NP77644.RAgCHEFNjEAJx3q3YuIuLie7BIDi2oGuNtvnwpDcGxF8M130_provenance a np:Provenance .
  
  dgn-np:NP77644.RAgCHEFNjEAJx3q3YuIuLie7BIDi2oGuNtvnwpDcGxF8M130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP77644.RAgCHEFNjEAJx3q3YuIuLie7BIDi2oGuNtvnwpDcGxF8M130_assertion {
  miriam-gene:1277 a ncit:C16612 .
  
  lld:C0021364 a ncit:C7057 .
  
  dgn-gda:DGN2ab7670fa767755dd882fb2c8e1cc8fd sio:SIO_000628 miriam-gene:1277, lld:C0021364;
    a sio:SIO_001122 .
}

dgn-np:NP77644.RAgCHEFNjEAJx3q3YuIuLie7BIDi2oGuNtvnwpDcGxF8M130_provenance {
  dgn-np:NP77644.RAgCHEFNjEAJx3q3YuIuLie7BIDi2oGuNtvnwpDcGxF8M130_assertion dcterms:description
      "[Our results suggest that variant alleles of the five markers are absent or too rare to be useful genetic makers in Chinese, despite the fact that they have been commonly used as polymorphic markers in osteoporosis genetic research in other populations.]. 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:12491092;
    prov:wasDerivedFrom dgn-void:gad-20150221;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP77644.RAgCHEFNjEAJx3q3YuIuLie7BIDi2oGuNtvnwpDcGxF8M130_publicationInfo {
  this: dcterms:created "2016-05-13T12:42:23+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}