@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP293661.RAyEzl5LpSDU71EMXoUb5gaHqQrNvRoBMcDRH3T82AzIo> .
@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:NP293661.RAyEzl5LpSDU71EMXoUb5gaHqQrNvRoBMcDRH3T82AzIo130_head {
  this: np:hasAssertion dgn-np:NP293661.RAyEzl5LpSDU71EMXoUb5gaHqQrNvRoBMcDRH3T82AzIo130_assertion;
    np:hasProvenance dgn-np:NP293661.RAyEzl5LpSDU71EMXoUb5gaHqQrNvRoBMcDRH3T82AzIo130_provenance;
    np:hasPublicationInfo dgn-np:NP293661.RAyEzl5LpSDU71EMXoUb5gaHqQrNvRoBMcDRH3T82AzIo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP293661.RAyEzl5LpSDU71EMXoUb5gaHqQrNvRoBMcDRH3T82AzIo130_assertion a np:Assertion .
  
  dgn-np:NP293661.RAyEzl5LpSDU71EMXoUb5gaHqQrNvRoBMcDRH3T82AzIo130_provenance a np:Provenance .
  
  dgn-np:NP293661.RAyEzl5LpSDU71EMXoUb5gaHqQrNvRoBMcDRH3T82AzIo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP293661.RAyEzl5LpSDU71EMXoUb5gaHqQrNvRoBMcDRH3T82AzIo130_assertion {
  miriam-gene:11186 a ncit:C16612 .
  
  lld:C0025286 a ncit:C7057 .
  
  dgn-gda:DGN71277bdd09519c0ac58db0b0a748af5f sio:SIO_000628 miriam-gene:11186, lld:C0025286;
    a sio:SIO_001121 .
}

dgn-np:NP293661.RAyEzl5LpSDU71EMXoUb5gaHqQrNvRoBMcDRH3T82AzIo130_provenance {
  dgn-np:NP293661.RAyEzl5LpSDU71EMXoUb5gaHqQrNvRoBMcDRH3T82AzIo130_assertion dcterms:description
      "[The aim of this study was to identify genes related to meningioma progression from the benign state to the atypical and anaplastic states by examining 1p LOH and the promoter methylation of RASSF1A and p73.]. 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:17695396;
    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:NP293661.RAyEzl5LpSDU71EMXoUb5gaHqQrNvRoBMcDRH3T82AzIo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:47+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" .
}