@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP563676.RAlCUDByUZyTaqkxi0UVrYj-qbR0nzDLTG6CmZKN6e4-w> .
@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:NP563676.RAlCUDByUZyTaqkxi0UVrYj-qbR0nzDLTG6CmZKN6e4-w130_head {
  this: np:hasAssertion dgn-np:NP563676.RAlCUDByUZyTaqkxi0UVrYj-qbR0nzDLTG6CmZKN6e4-w130_assertion;
    np:hasProvenance dgn-np:NP563676.RAlCUDByUZyTaqkxi0UVrYj-qbR0nzDLTG6CmZKN6e4-w130_provenance;
    np:hasPublicationInfo dgn-np:NP563676.RAlCUDByUZyTaqkxi0UVrYj-qbR0nzDLTG6CmZKN6e4-w130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP563676.RAlCUDByUZyTaqkxi0UVrYj-qbR0nzDLTG6CmZKN6e4-w130_assertion a np:Assertion .
  
  dgn-np:NP563676.RAlCUDByUZyTaqkxi0UVrYj-qbR0nzDLTG6CmZKN6e4-w130_provenance a np:Provenance .
  
  dgn-np:NP563676.RAlCUDByUZyTaqkxi0UVrYj-qbR0nzDLTG6CmZKN6e4-w130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP563676.RAlCUDByUZyTaqkxi0UVrYj-qbR0nzDLTG6CmZKN6e4-w130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  
  lld:C0206663 a ncit:C7057 .
  
  dgn-gda:DGN22fa221152330997b008c4d719221534 sio:SIO_000628 miriam-gene:7157, lld:C0206663;
    a sio:SIO_001121 .
}

dgn-np:NP563676.RAlCUDByUZyTaqkxi0UVrYj-qbR0nzDLTG6CmZKN6e4-w130_provenance {
  dgn-np:NP563676.RAlCUDByUZyTaqkxi0UVrYj-qbR0nzDLTG6CmZKN6e4-w130_assertion dcterms:description
      "[Cytogenetic and molecular analyses of primitive neuroectodermal tumors (PNETs) of the central nervous system (CNS) have demonstrated material losses of 17p, the region that contains the TP53 gene, as the most frequent abnormality.]. 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:9546059;
    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:NP563676.RAlCUDByUZyTaqkxi0UVrYj-qbR0nzDLTG6CmZKN6e4-w130_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" .
}