@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP844052.RAMQXl56NnIYFhDdDWBw6p2z5jxW92sYEXP14NNX7_Uyg> .
@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:NP844052.RAMQXl56NnIYFhDdDWBw6p2z5jxW92sYEXP14NNX7_Uyg130_head {
  this: np:hasAssertion dgn-np:NP844052.RAMQXl56NnIYFhDdDWBw6p2z5jxW92sYEXP14NNX7_Uyg130_assertion;
    np:hasProvenance dgn-np:NP844052.RAMQXl56NnIYFhDdDWBw6p2z5jxW92sYEXP14NNX7_Uyg130_provenance;
    np:hasPublicationInfo dgn-np:NP844052.RAMQXl56NnIYFhDdDWBw6p2z5jxW92sYEXP14NNX7_Uyg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP844052.RAMQXl56NnIYFhDdDWBw6p2z5jxW92sYEXP14NNX7_Uyg130_assertion a np:Assertion .
  
  dgn-np:NP844052.RAMQXl56NnIYFhDdDWBw6p2z5jxW92sYEXP14NNX7_Uyg130_provenance a np:Provenance .
  
  dgn-np:NP844052.RAMQXl56NnIYFhDdDWBw6p2z5jxW92sYEXP14NNX7_Uyg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP844052.RAMQXl56NnIYFhDdDWBw6p2z5jxW92sYEXP14NNX7_Uyg130_assertion {
  miriam-gene:6041 a ncit:C16612 .
  
  lld:C1704272 a ncit:C7057 .
  
  dgn-gda:DGN5e477482354e276e722aa701490f779b sio:SIO_000628 miriam-gene:6041, lld:C1704272;
    a sio:SIO_001121 .
}

dgn-np:NP844052.RAMQXl56NnIYFhDdDWBw6p2z5jxW92sYEXP14NNX7_Uyg130_provenance {
  dgn-np:NP844052.RAMQXl56NnIYFhDdDWBw6p2z5jxW92sYEXP14NNX7_Uyg130_assertion dcterms:description
      "[Here, we screened for RNASEL germline mutations in 66 Finnish patients with HPC, and we determined the frequency of the changes in the index patients from 116 families with HPC, in 492 patients with unselected prostate cancer (PRCA), in 223 patients with benign prostatic hyperplasia (BPH), and in 566 controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
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    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;
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}

dgn-np:NP844052.RAMQXl56NnIYFhDdDWBw6p2z5jxW92sYEXP14NNX7_Uyg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:36+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
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    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269>, <http://orcid.org/0000-0002-7534-7661>,
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}