@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP291155.RApbpymVzH7Vl1iBu9l-rJkcN_z2Z7_UnTVlB-dDw8ASY> .
@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:NP291155.RApbpymVzH7Vl1iBu9l-rJkcN_z2Z7_UnTVlB-dDw8ASY130_head {
  this: np:hasAssertion dgn-np:NP291155.RApbpymVzH7Vl1iBu9l-rJkcN_z2Z7_UnTVlB-dDw8ASY130_assertion;
    np:hasProvenance dgn-np:NP291155.RApbpymVzH7Vl1iBu9l-rJkcN_z2Z7_UnTVlB-dDw8ASY130_provenance;
    np:hasPublicationInfo dgn-np:NP291155.RApbpymVzH7Vl1iBu9l-rJkcN_z2Z7_UnTVlB-dDw8ASY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP291155.RApbpymVzH7Vl1iBu9l-rJkcN_z2Z7_UnTVlB-dDw8ASY130_assertion a np:Assertion .
  
  dgn-np:NP291155.RApbpymVzH7Vl1iBu9l-rJkcN_z2Z7_UnTVlB-dDw8ASY130_provenance a np:Provenance .
  
  dgn-np:NP291155.RApbpymVzH7Vl1iBu9l-rJkcN_z2Z7_UnTVlB-dDw8ASY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP291155.RApbpymVzH7Vl1iBu9l-rJkcN_z2Z7_UnTVlB-dDw8ASY130_assertion {
  miriam-gene:7161 a ncit:C16612 .
  
  lld:C0025286 a ncit:C7057 .
  
  dgn-gda:DGNf6d4ff6d76ed2e22d3ddc0dd43f52993 sio:SIO_000628 miriam-gene:7161, lld:C0025286;
    a sio:SIO_001121 .
}

dgn-np:NP291155.RApbpymVzH7Vl1iBu9l-rJkcN_z2Z7_UnTVlB-dDw8ASY130_provenance {
  dgn-np:NP291155.RApbpymVzH7Vl1iBu9l-rJkcN_z2Z7_UnTVlB-dDw8ASY130_assertion dcterms:description
      "[Based on the hypothesis that meningiomas cumulatively acquire genetic alterations and thus progress from the benign to the atypical and anaplastic states, genetic alterations in the methylation status of p73 or RASSF1A along with 1p LOH may result in the malignant transformation of a meningioma.]. 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:NP291155.RApbpymVzH7Vl1iBu9l-rJkcN_z2Z7_UnTVlB-dDw8ASY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:45+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" .
}