@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP45135.RAlVidoMI7s95XC-WA6b39UVG8UBp4CBLmCV3H_XeBPwo> .
@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 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:NP45135.RAlVidoMI7s95XC-WA6b39UVG8UBp4CBLmCV3H_XeBPwo130_head {
  this: np:hasAssertion dgn-np:NP45135.RAlVidoMI7s95XC-WA6b39UVG8UBp4CBLmCV3H_XeBPwo130_assertion;
    np:hasProvenance dgn-np:NP45135.RAlVidoMI7s95XC-WA6b39UVG8UBp4CBLmCV3H_XeBPwo130_provenance;
    np:hasPublicationInfo dgn-np:NP45135.RAlVidoMI7s95XC-WA6b39UVG8UBp4CBLmCV3H_XeBPwo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP45135.RAlVidoMI7s95XC-WA6b39UVG8UBp4CBLmCV3H_XeBPwo130_assertion a np:Assertion .
  
  dgn-np:NP45135.RAlVidoMI7s95XC-WA6b39UVG8UBp4CBLmCV3H_XeBPwo130_provenance a np:Provenance .
  
  dgn-np:NP45135.RAlVidoMI7s95XC-WA6b39UVG8UBp4CBLmCV3H_XeBPwo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP45135.RAlVidoMI7s95XC-WA6b39UVG8UBp4CBLmCV3H_XeBPwo130_assertion {
  miriam-gene:60528 a ncit:C16612 .
  
  lld:C0376358 a ncit:C7057 .
  
  dgn-gda:DGN3579ef7f9663cd7d8ce00b4d878775af sio:SIO_000628 miriam-gene:60528, lld:C0376358;
    a sio:SIO_001122 .
}

dgn-np:NP45135.RAlVidoMI7s95XC-WA6b39UVG8UBp4CBLmCV3H_XeBPwo130_provenance {
  dgn-np:NP45135.RAlVidoMI7s95XC-WA6b39UVG8UBp4CBLmCV3H_XeBPwo130_assertion dct:description
      "[ These results suggest that, in a European-American population, ELAC2 217L and RNASEL 541E are associated with metastatic sporadic disease. ELAC2 and RNASEL SNP analysis may prove useful in determining which patients are at risk for developing clinically significant prostate carcinoma.]. 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:16114055;
    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:NP45135.RAlVidoMI7s95XC-WA6b39UVG8UBp4CBLmCV3H_XeBPwo130_publicationInfo {
  this: dct:created "2014-10-02T12:32:20+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}