@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP311268.RAibnxLwkcSADgPBY5MmMXaCMfGY_86-86lcB5IeQEMok> .
@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:NP311268.RAibnxLwkcSADgPBY5MmMXaCMfGY_86-86lcB5IeQEMok130_head {
  this: np:hasAssertion dgn-np:NP311268.RAibnxLwkcSADgPBY5MmMXaCMfGY_86-86lcB5IeQEMok130_assertion;
    np:hasProvenance dgn-np:NP311268.RAibnxLwkcSADgPBY5MmMXaCMfGY_86-86lcB5IeQEMok130_provenance;
    np:hasPublicationInfo dgn-np:NP311268.RAibnxLwkcSADgPBY5MmMXaCMfGY_86-86lcB5IeQEMok130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP311268.RAibnxLwkcSADgPBY5MmMXaCMfGY_86-86lcB5IeQEMok130_assertion a np:Assertion .
  
  dgn-np:NP311268.RAibnxLwkcSADgPBY5MmMXaCMfGY_86-86lcB5IeQEMok130_provenance a np:Provenance .
  
  dgn-np:NP311268.RAibnxLwkcSADgPBY5MmMXaCMfGY_86-86lcB5IeQEMok130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP311268.RAibnxLwkcSADgPBY5MmMXaCMfGY_86-86lcB5IeQEMok130_assertion {
  miriam-gene:5655 a ncit:C16612 .
  
  lld:C0029925 a ncit:C7057 .
  
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    a sio:SIO_001121 .
}

dgn-np:NP311268.RAibnxLwkcSADgPBY5MmMXaCMfGY_86-86lcB5IeQEMok130_provenance {
  dgn-np:NP311268.RAibnxLwkcSADgPBY5MmMXaCMfGY_86-86lcB5IeQEMok130_assertion dcterms:description
      "[Potentially functional candidate KLK10 SNPs require investigation in future association studies of ovarian cancer risk and survival, including rs3760738 identified in aggressive ovarian cancer cell lines and predicted to affect transcription factor binding sites.]. 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:20686372;
    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:NP311268.RAibnxLwkcSADgPBY5MmMXaCMfGY_86-86lcB5IeQEMok130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:58+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}