@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP201017.RAdqdbqV2HA1mz_dCdOsOlE-gTfCaEK5yhV6uXSHmtUTc> .
@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:NP201017.RAdqdbqV2HA1mz_dCdOsOlE-gTfCaEK5yhV6uXSHmtUTc130_head {
  this: np:hasAssertion dgn-np:NP201017.RAdqdbqV2HA1mz_dCdOsOlE-gTfCaEK5yhV6uXSHmtUTc130_assertion;
    np:hasProvenance dgn-np:NP201017.RAdqdbqV2HA1mz_dCdOsOlE-gTfCaEK5yhV6uXSHmtUTc130_provenance;
    np:hasPublicationInfo dgn-np:NP201017.RAdqdbqV2HA1mz_dCdOsOlE-gTfCaEK5yhV6uXSHmtUTc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP201017.RAdqdbqV2HA1mz_dCdOsOlE-gTfCaEK5yhV6uXSHmtUTc130_assertion a np:Assertion .
  
  dgn-np:NP201017.RAdqdbqV2HA1mz_dCdOsOlE-gTfCaEK5yhV6uXSHmtUTc130_provenance a np:Provenance .
  
  dgn-np:NP201017.RAdqdbqV2HA1mz_dCdOsOlE-gTfCaEK5yhV6uXSHmtUTc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP201017.RAdqdbqV2HA1mz_dCdOsOlE-gTfCaEK5yhV6uXSHmtUTc130_assertion {
  miriam-gene:26038 a ncit:C16612 .
  
  lld:C0027819 a ncit:C7057 .
  
  dgn-gda:DGN4087bb8eb2cf358af8efe816c6e2fb4e sio:SIO_000628 miriam-gene:26038, lld:C0027819;
    a sio:SIO_001121 .
}

dgn-np:NP201017.RAdqdbqV2HA1mz_dCdOsOlE-gTfCaEK5yhV6uXSHmtUTc130_provenance {
  dgn-np:NP201017.RAdqdbqV2HA1mz_dCdOsOlE-gTfCaEK5yhV6uXSHmtUTc130_assertion dcterms:description
      "[Our mutation and expression analysis in neuroblastoma cell lines, combined with expression analysis in normal tissues, putative function and prior implication in neuroblastoma pathogenesis, suggests that the most promising TSG deleted from the 1p36 SRD is CHD5, but TNFRSF25, CAMTA1 and AJAP1 are also viable candidates.]. 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:17667943;
    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:NP201017.RAdqdbqV2HA1mz_dCdOsOlE-gTfCaEK5yhV6uXSHmtUTc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:51+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" .
}