@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1039300.RApgocg5S3YXn8ypsgcDj8XyAzaJ1F31Qh_NoK30IcgR0> .
@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:NP1039300.RApgocg5S3YXn8ypsgcDj8XyAzaJ1F31Qh_NoK30IcgR0130_head {
  this: np:hasAssertion dgn-np:NP1039300.RApgocg5S3YXn8ypsgcDj8XyAzaJ1F31Qh_NoK30IcgR0130_assertion;
    np:hasProvenance dgn-np:NP1039300.RApgocg5S3YXn8ypsgcDj8XyAzaJ1F31Qh_NoK30IcgR0130_provenance;
    np:hasPublicationInfo dgn-np:NP1039300.RApgocg5S3YXn8ypsgcDj8XyAzaJ1F31Qh_NoK30IcgR0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1039300.RApgocg5S3YXn8ypsgcDj8XyAzaJ1F31Qh_NoK30IcgR0130_assertion a np:Assertion .
  
  dgn-np:NP1039300.RApgocg5S3YXn8ypsgcDj8XyAzaJ1F31Qh_NoK30IcgR0130_provenance a np:Provenance .
  
  dgn-np:NP1039300.RApgocg5S3YXn8ypsgcDj8XyAzaJ1F31Qh_NoK30IcgR0130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1039300.RApgocg5S3YXn8ypsgcDj8XyAzaJ1F31Qh_NoK30IcgR0130_assertion {
  miriam-gene:4613 a ncit:C16612 .
  
  lld:C0700095 a ncit:C7057 .
  
  dgn-gda:DGN66b85bda390ddda1ee2d4bd3a7dbc34e sio:SIO_000628 miriam-gene:4613, lld:C0700095;
    a sio:SIO_001121 .
}

dgn-np:NP1039300.RApgocg5S3YXn8ypsgcDj8XyAzaJ1F31Qh_NoK30IcgR0130_provenance {
  dgn-np:NP1039300.RApgocg5S3YXn8ypsgcDj8XyAzaJ1F31Qh_NoK30IcgR0130_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;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}

dgn-np:NP1039300.RApgocg5S3YXn8ypsgcDj8XyAzaJ1F31Qh_NoK30IcgR0130_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;
    prv:usedData dgn-void:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}