@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP572321.RA8UVpv-O10exd2a8rjYIQJ2n_IMvyk-M4y_vmTBsUw0M> .
@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:NP572321.RA8UVpv-O10exd2a8rjYIQJ2n_IMvyk-M4y_vmTBsUw0M130_head {
  this: np:hasAssertion dgn-np:NP572321.RA8UVpv-O10exd2a8rjYIQJ2n_IMvyk-M4y_vmTBsUw0M130_assertion;
    np:hasProvenance dgn-np:NP572321.RA8UVpv-O10exd2a8rjYIQJ2n_IMvyk-M4y_vmTBsUw0M130_provenance;
    np:hasPublicationInfo dgn-np:NP572321.RA8UVpv-O10exd2a8rjYIQJ2n_IMvyk-M4y_vmTBsUw0M130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP572321.RA8UVpv-O10exd2a8rjYIQJ2n_IMvyk-M4y_vmTBsUw0M130_assertion a np:Assertion .
  
  dgn-np:NP572321.RA8UVpv-O10exd2a8rjYIQJ2n_IMvyk-M4y_vmTBsUw0M130_provenance a np:Provenance .
  
  dgn-np:NP572321.RA8UVpv-O10exd2a8rjYIQJ2n_IMvyk-M4y_vmTBsUw0M130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP572321.RA8UVpv-O10exd2a8rjYIQJ2n_IMvyk-M4y_vmTBsUw0M130_assertion {
  miriam-gene:10215 a ncit:C16612 .
  
  lld:C0014474 a ncit:C7057 .
  
  dgn-gda:DGNbd868c04e9a27f56766e33bcfde7a627 sio:SIO_000628 miriam-gene:10215, lld:C0014474;
    a sio:SIO_001121 .
}

dgn-np:NP572321.RA8UVpv-O10exd2a8rjYIQJ2n_IMvyk-M4y_vmTBsUw0M130_provenance {
  dgn-np:NP572321.RA8UVpv-O10exd2a8rjYIQJ2n_IMvyk-M4y_vmTBsUw0M130_assertion dcterms:description
      "[We analysed OLIG2 expression in 60 oligodendroglial neoplasms (57 with and three without chromosome 1p aberration), 10 central neurocytomas, 10 clear cell ependymomas, nine dysembryoplastic neuroepithelial tumours (DNTs) and two clear cell meningiomas using immunohistochemistry.]. 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:17257132;
    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:NP572321.RA8UVpv-O10exd2a8rjYIQJ2n_IMvyk-M4y_vmTBsUw0M130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:45+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" .
}