@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP362856.RAzwinCVrnEebHkcC9hAkpeM74UJXL14hwp_cQSyfpMKE> .
@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:NP362856.RAzwinCVrnEebHkcC9hAkpeM74UJXL14hwp_cQSyfpMKE130_head {
  this: np:hasAssertion dgn-np:NP362856.RAzwinCVrnEebHkcC9hAkpeM74UJXL14hwp_cQSyfpMKE130_assertion;
    np:hasProvenance dgn-np:NP362856.RAzwinCVrnEebHkcC9hAkpeM74UJXL14hwp_cQSyfpMKE130_provenance;
    np:hasPublicationInfo dgn-np:NP362856.RAzwinCVrnEebHkcC9hAkpeM74UJXL14hwp_cQSyfpMKE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP362856.RAzwinCVrnEebHkcC9hAkpeM74UJXL14hwp_cQSyfpMKE130_assertion a np:Assertion .
  
  dgn-np:NP362856.RAzwinCVrnEebHkcC9hAkpeM74UJXL14hwp_cQSyfpMKE130_provenance a np:Provenance .
  
  dgn-np:NP362856.RAzwinCVrnEebHkcC9hAkpeM74UJXL14hwp_cQSyfpMKE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP362856.RAzwinCVrnEebHkcC9hAkpeM74UJXL14hwp_cQSyfpMKE130_assertion {
  miriam-gene:4613 a ncit:C16612 .
  
  lld:C0006826 a ncit:C7057 .
  
  dgn-gda:DGN3d7691f2a4ab159069e290ba2a7da476 sio:SIO_000628 miriam-gene:4613, lld:C0006826;
    a sio:SIO_001121 .
}

dgn-np:NP362856.RAzwinCVrnEebHkcC9hAkpeM74UJXL14hwp_cQSyfpMKE130_provenance {
  dgn-np:NP362856.RAzwinCVrnEebHkcC9hAkpeM74UJXL14hwp_cQSyfpMKE130_assertion dcterms:description
      "[Loss of heterozygosity of the distal region of chromosome 1p where tumor suppressor gene(s) might harbor is frequently observed in many human cancers including neuroblastoma (NBL) with MYCN amplification and poor prognosis.]. 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:10980605;
    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:NP362856.RAzwinCVrnEebHkcC9hAkpeM74UJXL14hwp_cQSyfpMKE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:32+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" .
}