@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP873999.RAL8zKMyaYaBB-YcAsLydnqeJlII4ouv8x0uJVH_j4TFw> .
@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:NP873999.RAL8zKMyaYaBB-YcAsLydnqeJlII4ouv8x0uJVH_j4TFw130_head {
  this: np:hasAssertion dgn-np:NP873999.RAL8zKMyaYaBB-YcAsLydnqeJlII4ouv8x0uJVH_j4TFw130_assertion;
    np:hasProvenance dgn-np:NP873999.RAL8zKMyaYaBB-YcAsLydnqeJlII4ouv8x0uJVH_j4TFw130_provenance;
    np:hasPublicationInfo dgn-np:NP873999.RAL8zKMyaYaBB-YcAsLydnqeJlII4ouv8x0uJVH_j4TFw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP873999.RAL8zKMyaYaBB-YcAsLydnqeJlII4ouv8x0uJVH_j4TFw130_assertion a np:Assertion .
  
  dgn-np:NP873999.RAL8zKMyaYaBB-YcAsLydnqeJlII4ouv8x0uJVH_j4TFw130_provenance a np:Provenance .
  
  dgn-np:NP873999.RAL8zKMyaYaBB-YcAsLydnqeJlII4ouv8x0uJVH_j4TFw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP873999.RAL8zKMyaYaBB-YcAsLydnqeJlII4ouv8x0uJVH_j4TFw130_assertion {
  miriam-gene:6659 a ncit:C16612 .
  
  lld:C0006118 a ncit:C7057 .
  
  dgn-gda:DGNb60b2717a35cb8e5bf051e6402245d06 sio:SIO_000628 miriam-gene:6659, lld:C0006118;
    a sio:SIO_001121 .
}

dgn-np:NP873999.RAL8zKMyaYaBB-YcAsLydnqeJlII4ouv8x0uJVH_j4TFw130_provenance {
  dgn-np:NP873999.RAL8zKMyaYaBB-YcAsLydnqeJlII4ouv8x0uJVH_j4TFw130_assertion dcterms:description
      "[Furthermore, our findings support further analysis of the functional properties of the selected genes, especially SOX4 and BCAT1 for medulloblastoma and SOX9 for ependymoma, to evaluate the use of these genes as potential tumor markers, prognostic markers, and drug targets in pediatric brain tumors.]. 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:18577562;
    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:NP873999.RAL8zKMyaYaBB-YcAsLydnqeJlII4ouv8x0uJVH_j4TFw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:54+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" .
}