@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP292389.RAAsRPQ74SDhEnPqV8h50Gq2vqMB9n98h1E1rd27r8MDU> .
@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:NP292389.RAAsRPQ74SDhEnPqV8h50Gq2vqMB9n98h1E1rd27r8MDU130_head {
  this: np:hasAssertion dgn-np:NP292389.RAAsRPQ74SDhEnPqV8h50Gq2vqMB9n98h1E1rd27r8MDU130_assertion;
    np:hasProvenance dgn-np:NP292389.RAAsRPQ74SDhEnPqV8h50Gq2vqMB9n98h1E1rd27r8MDU130_provenance;
    np:hasPublicationInfo dgn-np:NP292389.RAAsRPQ74SDhEnPqV8h50Gq2vqMB9n98h1E1rd27r8MDU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP292389.RAAsRPQ74SDhEnPqV8h50Gq2vqMB9n98h1E1rd27r8MDU130_assertion a np:Assertion .
  
  dgn-np:NP292389.RAAsRPQ74SDhEnPqV8h50Gq2vqMB9n98h1E1rd27r8MDU130_provenance a np:Provenance .
  
  dgn-np:NP292389.RAAsRPQ74SDhEnPqV8h50Gq2vqMB9n98h1E1rd27r8MDU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP292389.RAAsRPQ74SDhEnPqV8h50Gq2vqMB9n98h1E1rd27r8MDU130_assertion {
  miriam-gene:5909 a ncit:C16612 .
  
  lld:C0549473 a ncit:C7057 .
  
  dgn-gda:DGNf740e8039f12e87b50164d9a5dd1bd71 sio:SIO_000628 miriam-gene:5909, lld:C0549473;
    a sio:SIO_001121 .
}

dgn-np:NP292389.RAAsRPQ74SDhEnPqV8h50Gq2vqMB9n98h1E1rd27r8MDU130_provenance {
  dgn-np:NP292389.RAAsRPQ74SDhEnPqV8h50Gq2vqMB9n98h1E1rd27r8MDU130_assertion dcterms:description
      "[In this study, we analyzed 197 thyroid tumor samples and showed that Rap1GAP was frequently lost or downregulated in various types of tumors, particularly in the most invasive and aggressive forms of thyroid cancer.]. 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:20124489;
    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:NP292389.RAAsRPQ74SDhEnPqV8h50Gq2vqMB9n98h1E1rd27r8MDU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:46+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" .
}