@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP60028.RAWCBQfvLoKAuRnCq7Cf7ATY5zJfdwhA20x4NUtJEL7ZA> .
@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:NP60028.RAWCBQfvLoKAuRnCq7Cf7ATY5zJfdwhA20x4NUtJEL7ZA130_head {
  this: np:hasAssertion dgn-np:NP60028.RAWCBQfvLoKAuRnCq7Cf7ATY5zJfdwhA20x4NUtJEL7ZA130_assertion;
    np:hasProvenance dgn-np:NP60028.RAWCBQfvLoKAuRnCq7Cf7ATY5zJfdwhA20x4NUtJEL7ZA130_provenance;
    np:hasPublicationInfo dgn-np:NP60028.RAWCBQfvLoKAuRnCq7Cf7ATY5zJfdwhA20x4NUtJEL7ZA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP60028.RAWCBQfvLoKAuRnCq7Cf7ATY5zJfdwhA20x4NUtJEL7ZA130_assertion a np:Assertion .
  
  dgn-np:NP60028.RAWCBQfvLoKAuRnCq7Cf7ATY5zJfdwhA20x4NUtJEL7ZA130_provenance a np:Provenance .
  
  dgn-np:NP60028.RAWCBQfvLoKAuRnCq7Cf7ATY5zJfdwhA20x4NUtJEL7ZA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP60028.RAWCBQfvLoKAuRnCq7Cf7ATY5zJfdwhA20x4NUtJEL7ZA130_assertion {
  miriam-gene:1565 a ncit:C16612 .
  
  lld:C0376358 a ncit:C7057 .
  
  dgn-gda:DGNd26c2273083949270fddb9086d9e6386 sio:SIO_000628 miriam-gene:1565, lld:C0376358;
    a sio:SIO_001122 .
}

dgn-np:NP60028.RAWCBQfvLoKAuRnCq7Cf7ATY5zJfdwhA20x4NUtJEL7ZA130_provenance {
  dgn-np:NP60028.RAWCBQfvLoKAuRnCq7Cf7ATY5zJfdwhA20x4NUtJEL7ZA130_assertion dcterms:description
      "[These observations have suggested that the CYP17 A2/A2, CYP1B1 Val/Val, and CYP2D6 genotypes may be associated with an altered risk of prostate cancer, while the CYP2D6 and SRD5A2 V89L polymorphism have no association with its risk in the North Indian population.]. 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:16716118;
    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:NP60028.RAWCBQfvLoKAuRnCq7Cf7ATY5zJfdwhA20x4NUtJEL7ZA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:28+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" .
}