@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP312033.RAqL06pOMCK7fA6_ijxFtfu8V5TKSdoOZPrzbyO9JsyS8> .
@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:NP312033.RAqL06pOMCK7fA6_ijxFtfu8V5TKSdoOZPrzbyO9JsyS8130_head {
  this: np:hasAssertion dgn-np:NP312033.RAqL06pOMCK7fA6_ijxFtfu8V5TKSdoOZPrzbyO9JsyS8130_assertion;
    np:hasProvenance dgn-np:NP312033.RAqL06pOMCK7fA6_ijxFtfu8V5TKSdoOZPrzbyO9JsyS8130_provenance;
    np:hasPublicationInfo dgn-np:NP312033.RAqL06pOMCK7fA6_ijxFtfu8V5TKSdoOZPrzbyO9JsyS8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP312033.RAqL06pOMCK7fA6_ijxFtfu8V5TKSdoOZPrzbyO9JsyS8130_assertion a np:Assertion .
  
  dgn-np:NP312033.RAqL06pOMCK7fA6_ijxFtfu8V5TKSdoOZPrzbyO9JsyS8130_provenance a np:Provenance .
  
  dgn-np:NP312033.RAqL06pOMCK7fA6_ijxFtfu8V5TKSdoOZPrzbyO9JsyS8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP312033.RAqL06pOMCK7fA6_ijxFtfu8V5TKSdoOZPrzbyO9JsyS8130_assertion {
  miriam-gene:3342 a ncit:C16612 .
  
  lld:C0376358 a ncit:C7057 .
  
  dgn-gda:DGNce39661f9494cd3a81dd563d4e91c47d sio:SIO_000628 miriam-gene:3342, lld:C0376358;
    a sio:SIO_001121 .
}

dgn-np:NP312033.RAqL06pOMCK7fA6_ijxFtfu8V5TKSdoOZPrzbyO9JsyS8130_provenance {
  dgn-np:NP312033.RAqL06pOMCK7fA6_ijxFtfu8V5TKSdoOZPrzbyO9JsyS8130_assertion dcterms:description
      "[Over the past 10 years, chromosomal aberrations in prostate cancer have been studied with several techniques, such as loss of heterozygosity (LOH), classical cytogenetics, and molecular cytogenetics, namely with fluorescence in situ hybridization (FISH) and comparative genomic hybridization (CGH).]. 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:11074616;
    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:NP312033.RAqL06pOMCK7fA6_ijxFtfu8V5TKSdoOZPrzbyO9JsyS8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:59+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" .
}