@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP765457.RAWO2Tx3DPXQr2ywAuveXD2YEnxyyjjefdQlGAi8xAiKs> .
@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:NP765457.RAWO2Tx3DPXQr2ywAuveXD2YEnxyyjjefdQlGAi8xAiKs130_head {
  this: np:hasAssertion dgn-np:NP765457.RAWO2Tx3DPXQr2ywAuveXD2YEnxyyjjefdQlGAi8xAiKs130_assertion;
    np:hasProvenance dgn-np:NP765457.RAWO2Tx3DPXQr2ywAuveXD2YEnxyyjjefdQlGAi8xAiKs130_provenance;
    np:hasPublicationInfo dgn-np:NP765457.RAWO2Tx3DPXQr2ywAuveXD2YEnxyyjjefdQlGAi8xAiKs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP765457.RAWO2Tx3DPXQr2ywAuveXD2YEnxyyjjefdQlGAi8xAiKs130_assertion a np:Assertion .
  
  dgn-np:NP765457.RAWO2Tx3DPXQr2ywAuveXD2YEnxyyjjefdQlGAi8xAiKs130_provenance a np:Provenance .
  
  dgn-np:NP765457.RAWO2Tx3DPXQr2ywAuveXD2YEnxyyjjefdQlGAi8xAiKs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP765457.RAWO2Tx3DPXQr2ywAuveXD2YEnxyyjjefdQlGAi8xAiKs130_assertion {
  miriam-gene:8874 a ncit:C16612 .
  
  lld:C0007097 a ncit:C7057 .
  
  dgn-gda:DGNf4944d92ee7fd9f4c2f40be5802e0060 sio:SIO_000628 miriam-gene:8874, lld:C0007097;
    a sio:SIO_001121 .
}

dgn-np:NP765457.RAWO2Tx3DPXQr2ywAuveXD2YEnxyyjjefdQlGAi8xAiKs130_provenance {
  dgn-np:NP765457.RAWO2Tx3DPXQr2ywAuveXD2YEnxyyjjefdQlGAi8xAiKs130_assertion dcterms:description
      "[We recently suggested that, besides their origin in the ovary, reduction of CDC42 messenger RNA (a member of the RHO GTPase family) may contribute to explain why clear cell carcinomas are not uncommonly found limited to the ovary (stage I).]. 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:21944080;
    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:NP765457.RAWO2Tx3DPXQr2ywAuveXD2YEnxyyjjefdQlGAi8xAiKs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:43+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" .
}