@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP260949.RATkv47NIWzv_PfKMsxXoiXF05Oi0uzfge-oGPEhJFVyY> .
@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:NP260949.RATkv47NIWzv_PfKMsxXoiXF05Oi0uzfge-oGPEhJFVyY130_head {
  this: np:hasAssertion dgn-np:NP260949.RATkv47NIWzv_PfKMsxXoiXF05Oi0uzfge-oGPEhJFVyY130_assertion;
    np:hasProvenance dgn-np:NP260949.RATkv47NIWzv_PfKMsxXoiXF05Oi0uzfge-oGPEhJFVyY130_provenance;
    np:hasPublicationInfo dgn-np:NP260949.RATkv47NIWzv_PfKMsxXoiXF05Oi0uzfge-oGPEhJFVyY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP260949.RATkv47NIWzv_PfKMsxXoiXF05Oi0uzfge-oGPEhJFVyY130_assertion a np:Assertion .
  
  dgn-np:NP260949.RATkv47NIWzv_PfKMsxXoiXF05Oi0uzfge-oGPEhJFVyY130_provenance a np:Provenance .
  
  dgn-np:NP260949.RATkv47NIWzv_PfKMsxXoiXF05Oi0uzfge-oGPEhJFVyY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP260949.RATkv47NIWzv_PfKMsxXoiXF05Oi0uzfge-oGPEhJFVyY130_assertion {
  miriam-gene:5460 a ncit:C16612 .
  
  lld:C0027654 a ncit:C7057 .
  
  dgn-gda:DGN56b42e6d1907628f9c7d63dc5fcc6770 sio:SIO_000628 miriam-gene:5460, lld:C0027654;
    a sio:SIO_001121 .
}

dgn-np:NP260949.RATkv47NIWzv_PfKMsxXoiXF05Oi0uzfge-oGPEhJFVyY130_provenance {
  dgn-np:NP260949.RATkv47NIWzv_PfKMsxXoiXF05Oi0uzfge-oGPEhJFVyY130_assertion dcterms:description
      "[Here, we investigated expression and prognostic value of the neural stem cell marker CD133, as well as of the pluripotency genes LIN28 and OCT4 in 37 samples of pediatric medulloblastoma, the most common and challenging type of embryonal tumor.]. 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:21725800;
    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:NP260949.RATkv47NIWzv_PfKMsxXoiXF05Oi0uzfge-oGPEhJFVyY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:25+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" .
}