@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP682631.RAH_dhGZM1VPic9M_TmwfDNXT0MAJTSH5h4taLJ3A_vGM> .
@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:NP682631.RAH_dhGZM1VPic9M_TmwfDNXT0MAJTSH5h4taLJ3A_vGM130_head {
  this: np:hasAssertion dgn-np:NP682631.RAH_dhGZM1VPic9M_TmwfDNXT0MAJTSH5h4taLJ3A_vGM130_assertion;
    np:hasProvenance dgn-np:NP682631.RAH_dhGZM1VPic9M_TmwfDNXT0MAJTSH5h4taLJ3A_vGM130_provenance;
    np:hasPublicationInfo dgn-np:NP682631.RAH_dhGZM1VPic9M_TmwfDNXT0MAJTSH5h4taLJ3A_vGM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP682631.RAH_dhGZM1VPic9M_TmwfDNXT0MAJTSH5h4taLJ3A_vGM130_assertion a np:Assertion .
  
  dgn-np:NP682631.RAH_dhGZM1VPic9M_TmwfDNXT0MAJTSH5h4taLJ3A_vGM130_provenance a np:Provenance .
  
  dgn-np:NP682631.RAH_dhGZM1VPic9M_TmwfDNXT0MAJTSH5h4taLJ3A_vGM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP682631.RAH_dhGZM1VPic9M_TmwfDNXT0MAJTSH5h4taLJ3A_vGM130_assertion {
  miriam-gene:799 a ncit:C16612 .
  
  lld:C0007847 a ncit:C7057 .
  
  dgn-gda:DGN48dcf8007f0171b5cd1ee10c73fff9ab sio:SIO_000628 miriam-gene:799, lld:C0007847;
    a sio:SIO_001121 .
}

dgn-np:NP682631.RAH_dhGZM1VPic9M_TmwfDNXT0MAJTSH5h4taLJ3A_vGM130_provenance {
  dgn-np:NP682631.RAH_dhGZM1VPic9M_TmwfDNXT0MAJTSH5h4taLJ3A_vGM130_assertion dcterms:description
      "[The aims of this study were (1) to evaluate the frequency of PIK3CA mutations in patients with cervical cancer treated with radical CRT and (2) to examine the effect of tumor PIK3CA mutational status in pre-treatment biopsies on overall survival (OS) and progression-free survival (PFS).]. 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:23266353;
    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:NP682631.RAH_dhGZM1VPic9M_TmwfDNXT0MAJTSH5h4taLJ3A_vGM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:55+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" .
}