@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP345618.RAgfVqsg8oyf_O6vF6Y1qNB_EgaWPKVZn1EX0uSXyQsf4> .
@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:NP345618.RAgfVqsg8oyf_O6vF6Y1qNB_EgaWPKVZn1EX0uSXyQsf4130_head {
  this: np:hasAssertion dgn-np:NP345618.RAgfVqsg8oyf_O6vF6Y1qNB_EgaWPKVZn1EX0uSXyQsf4130_assertion;
    np:hasProvenance dgn-np:NP345618.RAgfVqsg8oyf_O6vF6Y1qNB_EgaWPKVZn1EX0uSXyQsf4130_provenance;
    np:hasPublicationInfo dgn-np:NP345618.RAgfVqsg8oyf_O6vF6Y1qNB_EgaWPKVZn1EX0uSXyQsf4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP345618.RAgfVqsg8oyf_O6vF6Y1qNB_EgaWPKVZn1EX0uSXyQsf4130_assertion a np:Assertion .
  
  dgn-np:NP345618.RAgfVqsg8oyf_O6vF6Y1qNB_EgaWPKVZn1EX0uSXyQsf4130_provenance a np:Provenance .
  
  dgn-np:NP345618.RAgfVqsg8oyf_O6vF6Y1qNB_EgaWPKVZn1EX0uSXyQsf4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP345618.RAgfVqsg8oyf_O6vF6Y1qNB_EgaWPKVZn1EX0uSXyQsf4130_assertion {
  miriam-gene:5728 a ncit:C16612 .
  
  lld:C0206726 a ncit:C7057 .
  
  dgn-gda:DGNd540ad48e0f8c2dc1fc9496d3ec4f703 sio:SIO_000628 miriam-gene:5728, lld:C0206726;
    a sio:SIO_001121 .
}

dgn-np:NP345618.RAgfVqsg8oyf_O6vF6Y1qNB_EgaWPKVZn1EX0uSXyQsf4130_provenance {
  dgn-np:NP345618.RAgfVqsg8oyf_O6vF6Y1qNB_EgaWPKVZn1EX0uSXyQsf4130_assertion dcterms:description
      "[Unusual findings include: TP53 mutation in a juvenile pilocytic astrocytoma; TP53 and PTEN mutations in a de novo glioblastoma, a gliosarcoma with identical mutations in gliomatous and sarcomatous components, and an infratentorial anaplastic astrocytoma with an earlier supratentorial grade II astrocytoma bearing the same TP53 mutation but not the PTEN mutation or loss of heterozygosity (LOH) of 10q23.]. 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:11355303;
    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:NP345618.RAgfVqsg8oyf_O6vF6Y1qNB_EgaWPKVZn1EX0uSXyQsf4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:23+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" .
}