@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1039298.RAjPDvOuPD-5sAk1CABpqH8T90o437g_1fQoMNRnwIV2U> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .
dgn-np:NP1039298.RAjPDvOuPD-5sAk1CABpqH8T90o437g_1fQoMNRnwIV2U130_head {
  this: np:hasAssertion dgn-np:NP1039298.RAjPDvOuPD-5sAk1CABpqH8T90o437g_1fQoMNRnwIV2U130_assertion ;
    np:hasProvenance dgn-np:NP1039298.RAjPDvOuPD-5sAk1CABpqH8T90o437g_1fQoMNRnwIV2U130_provenance ;
    np:hasPublicationInfo dgn-np:NP1039298.RAjPDvOuPD-5sAk1CABpqH8T90o437g_1fQoMNRnwIV2U130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP1039298.RAjPDvOuPD-5sAk1CABpqH8T90o437g_1fQoMNRnwIV2U130_provenance a np:Provenance .
  dgn-np:NP1039298.RAjPDvOuPD-5sAk1CABpqH8T90o437g_1fQoMNRnwIV2U130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP1039298.RAjPDvOuPD-5sAk1CABpqH8T90o437g_1fQoMNRnwIV2U130_assertion {
  miriam-gene:4613 a ncit:C16612 .
  lld:C0027819 a ncit:C7057 .
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}
dgn-np:NP1039298.RAjPDvOuPD-5sAk1CABpqH8T90o437g_1fQoMNRnwIV2U130_provenance {
  dgn-np:NP1039298.RAjPDvOuPD-5sAk1CABpqH8T90o437g_1fQoMNRnwIV2U130_assertion dcterms:description "[Genomic amplification of the MYCN oncogene has been used to predict outcome in neuroblastoma for over 30 years, however, recent methodological advances including miRNA and mRNA profiling, comparative genomic hybridization (array-CGH), and whole-genome sequencing have enabled the detailed analysis of the neuroblastoma genome, leading to the identification of new prognostic markers and better patient stratification.]. 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:23274701 ;
    prov:wasDerivedFrom dgn-void:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1039298.RAjPDvOuPD-5sAk1CABpqH8T90o437g_1fQoMNRnwIV2U130_publicationInfo {
  this: dcterms:created "2016-05-13T12:49:37+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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}