@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP234939.RAGv1uEfPMbi0TvRtWdnaf8coZDUetGWFx3Z5ael-CGvs> .
@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:NP234939.RAGv1uEfPMbi0TvRtWdnaf8coZDUetGWFx3Z5ael-CGvs130_head {
  this: np:hasAssertion dgn-np:NP234939.RAGv1uEfPMbi0TvRtWdnaf8coZDUetGWFx3Z5ael-CGvs130_assertion;
    np:hasProvenance dgn-np:NP234939.RAGv1uEfPMbi0TvRtWdnaf8coZDUetGWFx3Z5ael-CGvs130_provenance;
    np:hasPublicationInfo dgn-np:NP234939.RAGv1uEfPMbi0TvRtWdnaf8coZDUetGWFx3Z5ael-CGvs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP234939.RAGv1uEfPMbi0TvRtWdnaf8coZDUetGWFx3Z5ael-CGvs130_assertion a np:Assertion .
  
  dgn-np:NP234939.RAGv1uEfPMbi0TvRtWdnaf8coZDUetGWFx3Z5ael-CGvs130_provenance a np:Provenance .
  
  dgn-np:NP234939.RAGv1uEfPMbi0TvRtWdnaf8coZDUetGWFx3Z5ael-CGvs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP234939.RAGv1uEfPMbi0TvRtWdnaf8coZDUetGWFx3Z5ael-CGvs130_assertion {
  miriam-gene:1871 a ncit:C16612 .
  
  lld:C1266186 a ncit:C7057 .
  
  dgn-gda:DGNa70affc3626da353e655dbbb83597c69 sio:SIO_000628 miriam-gene:1871, lld:C1266186;
    a sio:SIO_001121 .
}

dgn-np:NP234939.RAGv1uEfPMbi0TvRtWdnaf8coZDUetGWFx3Z5ael-CGvs130_provenance {
  dgn-np:NP234939.RAGv1uEfPMbi0TvRtWdnaf8coZDUetGWFx3Z5ael-CGvs130_assertion dcterms:description
      "[Our results suggest that MDM4 gain may be involved in the early transition from normal retina to retinoma, while MYCN and E2F3 progressive gain may represent driving factors of tumor progression.]. 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:18785023;
    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:NP234939.RAGv1uEfPMbi0TvRtWdnaf8coZDUetGWFx3Z5ael-CGvs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:12+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" .
}