@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP925791.RAC-bqDOETB7YAy8HAWsj6V05CtiOoLmwdr6IfEWM-RLE> .
@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:NP925791.RAC-bqDOETB7YAy8HAWsj6V05CtiOoLmwdr6IfEWM-RLE130_head {
  this: np:hasAssertion dgn-np:NP925791.RAC-bqDOETB7YAy8HAWsj6V05CtiOoLmwdr6IfEWM-RLE130_assertion;
    np:hasProvenance dgn-np:NP925791.RAC-bqDOETB7YAy8HAWsj6V05CtiOoLmwdr6IfEWM-RLE130_provenance;
    np:hasPublicationInfo dgn-np:NP925791.RAC-bqDOETB7YAy8HAWsj6V05CtiOoLmwdr6IfEWM-RLE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP925791.RAC-bqDOETB7YAy8HAWsj6V05CtiOoLmwdr6IfEWM-RLE130_assertion a np:Assertion .
  
  dgn-np:NP925791.RAC-bqDOETB7YAy8HAWsj6V05CtiOoLmwdr6IfEWM-RLE130_provenance a np:Provenance .
  
  dgn-np:NP925791.RAC-bqDOETB7YAy8HAWsj6V05CtiOoLmwdr6IfEWM-RLE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP925791.RAC-bqDOETB7YAy8HAWsj6V05CtiOoLmwdr6IfEWM-RLE130_assertion {
  miriam-gene:342977 a ncit:C16612 .
  
  lld:C0521170 a ncit:C7057 .
  
  dgn-gda:DGN31b771bfc283876a5bcce3637170b713 sio:SIO_000628 miriam-gene:342977, lld:C0521170;
    a sio:SIO_001121 .
}

dgn-np:NP925791.RAC-bqDOETB7YAy8HAWsj6V05CtiOoLmwdr6IfEWM-RLE130_provenance {
  dgn-np:NP925791.RAC-bqDOETB7YAy8HAWsj6V05CtiOoLmwdr6IfEWM-RLE130_assertion dcterms:description
      "[We examined the associations between the Glu298Asp polymorphism of NOS3, indices of bone strength, and the incidence of fracture among 6691 women aged 65 years and older enrolled in the Study of Osteoporotic Fractures.]. 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:16503213;
    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:NP925791.RAC-bqDOETB7YAy8HAWsj6V05CtiOoLmwdr6IfEWM-RLE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:28+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" .
}