@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP564611.RA-mXXwnO2FP5L_KB2E5nJC_SWlLazW0AiskDREEvjQrY> .
@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:NP564611.RA-mXXwnO2FP5L_KB2E5nJC_SWlLazW0AiskDREEvjQrY130_head {
  this: np:hasAssertion dgn-np:NP564611.RA-mXXwnO2FP5L_KB2E5nJC_SWlLazW0AiskDREEvjQrY130_assertion;
    np:hasProvenance dgn-np:NP564611.RA-mXXwnO2FP5L_KB2E5nJC_SWlLazW0AiskDREEvjQrY130_provenance;
    np:hasPublicationInfo dgn-np:NP564611.RA-mXXwnO2FP5L_KB2E5nJC_SWlLazW0AiskDREEvjQrY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP564611.RA-mXXwnO2FP5L_KB2E5nJC_SWlLazW0AiskDREEvjQrY130_assertion a np:Assertion .
  
  dgn-np:NP564611.RA-mXXwnO2FP5L_KB2E5nJC_SWlLazW0AiskDREEvjQrY130_provenance a np:Provenance .
  
  dgn-np:NP564611.RA-mXXwnO2FP5L_KB2E5nJC_SWlLazW0AiskDREEvjQrY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP564611.RA-mXXwnO2FP5L_KB2E5nJC_SWlLazW0AiskDREEvjQrY130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  
  lld:C0431108 a ncit:C7057 .
  
  dgn-gda:DGNa796d3fb42ed198433010c1d8d13affc sio:SIO_000628 miriam-gene:7157, lld:C0431108;
    a sio:SIO_001121 .
}

dgn-np:NP564611.RA-mXXwnO2FP5L_KB2E5nJC_SWlLazW0AiskDREEvjQrY130_provenance {
  dgn-np:NP564611.RA-mXXwnO2FP5L_KB2E5nJC_SWlLazW0AiskDREEvjQrY130_assertion dcterms:description
      "[To test the possibility of regional molecular heterogeneity in oligoastrocytoma, we examined a series of 203 gliomas including 68 oligoastrocytomas and two control groups of 73 oligodendrogliomas and 62 astrocytomas for allelic losses of chromosomal arms 1p and 19q, and TP53 mutations, and compared these data with tumor localization.]. 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:12107116;
    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:NP564611.RA-mXXwnO2FP5L_KB2E5nJC_SWlLazW0AiskDREEvjQrY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:40+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" .
}