@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP818543.RALtwoq9AmJ3rM7A2uXpLL0SFlCNL7odDXy4VricYZELc> .
@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:NP818543.RALtwoq9AmJ3rM7A2uXpLL0SFlCNL7odDXy4VricYZELc130_head {
  this: np:hasAssertion dgn-np:NP818543.RALtwoq9AmJ3rM7A2uXpLL0SFlCNL7odDXy4VricYZELc130_assertion ;
    np:hasProvenance dgn-np:NP818543.RALtwoq9AmJ3rM7A2uXpLL0SFlCNL7odDXy4VricYZELc130_provenance ;
    np:hasPublicationInfo dgn-np:NP818543.RALtwoq9AmJ3rM7A2uXpLL0SFlCNL7odDXy4VricYZELc130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP818543.RALtwoq9AmJ3rM7A2uXpLL0SFlCNL7odDXy4VricYZELc130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP818543.RALtwoq9AmJ3rM7A2uXpLL0SFlCNL7odDXy4VricYZELc130_assertion {
  miriam-gene:4609 a ncit:C16612 .
  lld:C0029925 a ncit:C7057 .
  dgn-gda:DGNff396029eff76a7102741a18e36e4dc2 sio:SIO_000628 miriam-gene:4609 , lld:C0029925 ;
    a sio:SIO_001121 .
}
dgn-np:NP818543.RALtwoq9AmJ3rM7A2uXpLL0SFlCNL7odDXy4VricYZELc130_provenance {
  dgn-np:NP818543.RALtwoq9AmJ3rM7A2uXpLL0SFlCNL7odDXy4VricYZELc130_assertion dcterms:description "[To accomplish this, we assessed the association of amplification at 8q24 with outcome in ovarian cancers using fluorescence in situ hybridization to tissue microarrays and measured responses of ovarian and breast cancer cell lines to specific small interfering RNAs against the oncogene MYC and a putative noncoding RNA, PVT1, both of which map to 8q24.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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    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 ;
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}
dgn-np:NP818543.RALtwoq9AmJ3rM7A2uXpLL0SFlCNL7odDXy4VricYZELc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:21+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
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}