@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP876106.RA8yu5FArNKW8dHSkpfQ4RhXiH4Obel-fcKQRspCo2wGY> .
@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:NP876106.RA8yu5FArNKW8dHSkpfQ4RhXiH4Obel-fcKQRspCo2wGY130_head {
  this: np:hasAssertion dgn-np:NP876106.RA8yu5FArNKW8dHSkpfQ4RhXiH4Obel-fcKQRspCo2wGY130_assertion;
    np:hasProvenance dgn-np:NP876106.RA8yu5FArNKW8dHSkpfQ4RhXiH4Obel-fcKQRspCo2wGY130_provenance;
    np:hasPublicationInfo dgn-np:NP876106.RA8yu5FArNKW8dHSkpfQ4RhXiH4Obel-fcKQRspCo2wGY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP876106.RA8yu5FArNKW8dHSkpfQ4RhXiH4Obel-fcKQRspCo2wGY130_assertion a np:Assertion .
  
  dgn-np:NP876106.RA8yu5FArNKW8dHSkpfQ4RhXiH4Obel-fcKQRspCo2wGY130_provenance a np:Provenance .
  
  dgn-np:NP876106.RA8yu5FArNKW8dHSkpfQ4RhXiH4Obel-fcKQRspCo2wGY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP876106.RA8yu5FArNKW8dHSkpfQ4RhXiH4Obel-fcKQRspCo2wGY130_assertion {
  miriam-gene:3918 a ncit:C16612 .
  
  lld:C1458156 a ncit:C7057 .
  
  dgn-gda:DGNcca661ce4562390925d60c2149d85250 sio:SIO_000628 miriam-gene:3918, lld:C1458156;
    a sio:SIO_001121 .
}

dgn-np:NP876106.RA8yu5FArNKW8dHSkpfQ4RhXiH4Obel-fcKQRspCo2wGY130_provenance {
  dgn-np:NP876106.RA8yu5FArNKW8dHSkpfQ4RhXiH4Obel-fcKQRspCo2wGY130_assertion dcterms:description
      "[The PNET may be amenable in the future to gene therapy strategies because of its rapid proliferative potential, its tendency to spread within the CSF pathways, and its high recurrence rate.]. 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:8817422;
    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:NP876106.RA8yu5FArNKW8dHSkpfQ4RhXiH4Obel-fcKQRspCo2wGY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:55+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" .
}