@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP61035.RAaNhwik2JhGeM8PjV2nkOGVuBny02QdyI1e0WssfrxEU> .
@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:NP61035.RAaNhwik2JhGeM8PjV2nkOGVuBny02QdyI1e0WssfrxEU130_head {
  this: np:hasAssertion dgn-np:NP61035.RAaNhwik2JhGeM8PjV2nkOGVuBny02QdyI1e0WssfrxEU130_assertion;
    np:hasProvenance dgn-np:NP61035.RAaNhwik2JhGeM8PjV2nkOGVuBny02QdyI1e0WssfrxEU130_provenance;
    np:hasPublicationInfo dgn-np:NP61035.RAaNhwik2JhGeM8PjV2nkOGVuBny02QdyI1e0WssfrxEU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP61035.RAaNhwik2JhGeM8PjV2nkOGVuBny02QdyI1e0WssfrxEU130_assertion a np:Assertion .
  
  dgn-np:NP61035.RAaNhwik2JhGeM8PjV2nkOGVuBny02QdyI1e0WssfrxEU130_provenance a np:Provenance .
  
  dgn-np:NP61035.RAaNhwik2JhGeM8PjV2nkOGVuBny02QdyI1e0WssfrxEU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP61035.RAaNhwik2JhGeM8PjV2nkOGVuBny02QdyI1e0WssfrxEU130_assertion {
  miriam-gene:3569 a ncit:C16612 .
  
  lld:C0021364 a ncit:C7057 .
  
  dgn-gda:DGN3c2d0ed778849b404d736167a1947f95 sio:SIO_000628 miriam-gene:3569, lld:C0021364;
    a sio:SIO_001122 .
}

dgn-np:NP61035.RAaNhwik2JhGeM8PjV2nkOGVuBny02QdyI1e0WssfrxEU130_provenance {
  dgn-np:NP61035.RAaNhwik2JhGeM8PjV2nkOGVuBny02QdyI1e0WssfrxEU130_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-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:NP61035.RAaNhwik2JhGeM8PjV2nkOGVuBny02QdyI1e0WssfrxEU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:29+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" .
}