@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP343401.RA7zHNTyo8tPBbI27ejKF1d3hz6tilWwWmlZvYOjGmNUY> .
@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:NP343401.RA7zHNTyo8tPBbI27ejKF1d3hz6tilWwWmlZvYOjGmNUY130_head {
  this: np:hasAssertion dgn-np:NP343401.RA7zHNTyo8tPBbI27ejKF1d3hz6tilWwWmlZvYOjGmNUY130_assertion;
    np:hasProvenance dgn-np:NP343401.RA7zHNTyo8tPBbI27ejKF1d3hz6tilWwWmlZvYOjGmNUY130_provenance;
    np:hasPublicationInfo dgn-np:NP343401.RA7zHNTyo8tPBbI27ejKF1d3hz6tilWwWmlZvYOjGmNUY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP343401.RA7zHNTyo8tPBbI27ejKF1d3hz6tilWwWmlZvYOjGmNUY130_assertion a np:Assertion .
  
  dgn-np:NP343401.RA7zHNTyo8tPBbI27ejKF1d3hz6tilWwWmlZvYOjGmNUY130_provenance a np:Provenance .
  
  dgn-np:NP343401.RA7zHNTyo8tPBbI27ejKF1d3hz6tilWwWmlZvYOjGmNUY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP343401.RA7zHNTyo8tPBbI27ejKF1d3hz6tilWwWmlZvYOjGmNUY130_assertion {
  miriam-gene:1029 a ncit:C16612 .
  
  lld:C0700095 a ncit:C7057 .
  
  dgn-gda:DGNe4c0f82aab31f36a8033a94674656950 sio:SIO_000628 miriam-gene:1029, lld:C0700095;
    a sio:SIO_001121 .
}

dgn-np:NP343401.RA7zHNTyo8tPBbI27ejKF1d3hz6tilWwWmlZvYOjGmNUY130_provenance {
  dgn-np:NP343401.RA7zHNTyo8tPBbI27ejKF1d3hz6tilWwWmlZvYOjGmNUY130_assertion dcterms:description
      "[We previously reported that loss of heterozygosity (LOH) on chromosome 9p21 correlates with poor prognosis of neuroblastoma and the p16 gene is not expressed in approximately two thirds of neuroblastoma cell lines.]. 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:9872329;
    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:NP343401.RA7zHNTyo8tPBbI27ejKF1d3hz6tilWwWmlZvYOjGmNUY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:22+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" .
}