@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP339593.RACGB_IUEZU8KOS1zmL2MG3RLwRWHic-ybYKEsi9ss3nU> .
@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:NP339593.RACGB_IUEZU8KOS1zmL2MG3RLwRWHic-ybYKEsi9ss3nU130_head {
  this: np:hasAssertion dgn-np:NP339593.RACGB_IUEZU8KOS1zmL2MG3RLwRWHic-ybYKEsi9ss3nU130_assertion;
    np:hasProvenance dgn-np:NP339593.RACGB_IUEZU8KOS1zmL2MG3RLwRWHic-ybYKEsi9ss3nU130_provenance;
    np:hasPublicationInfo dgn-np:NP339593.RACGB_IUEZU8KOS1zmL2MG3RLwRWHic-ybYKEsi9ss3nU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP339593.RACGB_IUEZU8KOS1zmL2MG3RLwRWHic-ybYKEsi9ss3nU130_assertion a np:Assertion .
  
  dgn-np:NP339593.RACGB_IUEZU8KOS1zmL2MG3RLwRWHic-ybYKEsi9ss3nU130_provenance a np:Provenance .
  
  dgn-np:NP339593.RACGB_IUEZU8KOS1zmL2MG3RLwRWHic-ybYKEsi9ss3nU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP339593.RACGB_IUEZU8KOS1zmL2MG3RLwRWHic-ybYKEsi9ss3nU130_assertion {
  miriam-gene:7015 a ncit:C16612 .
  
  lld:C0029925 a ncit:C7057 .
  
  dgn-gda:DGN721db094393517ddd2f1880d8eda049b sio:SIO_000628 miriam-gene:7015, lld:C0029925;
    a sio:SIO_001121 .
}

dgn-np:NP339593.RACGB_IUEZU8KOS1zmL2MG3RLwRWHic-ybYKEsi9ss3nU130_provenance {
  dgn-np:NP339593.RACGB_IUEZU8KOS1zmL2MG3RLwRWHic-ybYKEsi9ss3nU130_assertion dcterms:description
      "[As both Rb and hTERT pathways are commonly altered in human ovarian cancer and these genetic changes are faithfully modeled in these cells without using viral protein, these immortal cells represent an authentic in vitro model system with which to study the initiation and progression of human ovarian cancer.]. 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:16953228;
    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:NP339593.RACGB_IUEZU8KOS1zmL2MG3RLwRWHic-ybYKEsi9ss3nU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:19+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" .
}