@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP222186.RAcqYv4Gk7M3L-z4QotkTf6N1GWfH1qCs9NV3yduqUKdc> .
@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:NP222186.RAcqYv4Gk7M3L-z4QotkTf6N1GWfH1qCs9NV3yduqUKdc130_head {
  this: np:hasAssertion dgn-np:NP222186.RAcqYv4Gk7M3L-z4QotkTf6N1GWfH1qCs9NV3yduqUKdc130_assertion;
    np:hasProvenance dgn-np:NP222186.RAcqYv4Gk7M3L-z4QotkTf6N1GWfH1qCs9NV3yduqUKdc130_provenance;
    np:hasPublicationInfo dgn-np:NP222186.RAcqYv4Gk7M3L-z4QotkTf6N1GWfH1qCs9NV3yduqUKdc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP222186.RAcqYv4Gk7M3L-z4QotkTf6N1GWfH1qCs9NV3yduqUKdc130_assertion a np:Assertion .
  
  dgn-np:NP222186.RAcqYv4Gk7M3L-z4QotkTf6N1GWfH1qCs9NV3yduqUKdc130_provenance a np:Provenance .
  
  dgn-np:NP222186.RAcqYv4Gk7M3L-z4QotkTf6N1GWfH1qCs9NV3yduqUKdc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP222186.RAcqYv4Gk7M3L-z4QotkTf6N1GWfH1qCs9NV3yduqUKdc130_assertion {
  miriam-gene:5519 a ncit:C16612 .
  
  lld:C0029925 a ncit:C7057 .
  
  dgn-gda:DGN88aee692db259e2735d862b6295f34b2 sio:SIO_000628 miriam-gene:5519, lld:C0029925;
    a sio:SIO_001121 .
}

dgn-np:NP222186.RAcqYv4Gk7M3L-z4QotkTf6N1GWfH1qCs9NV3yduqUKdc130_provenance {
  dgn-np:NP222186.RAcqYv4Gk7M3L-z4QotkTf6N1GWfH1qCs9NV3yduqUKdc130_assertion dcterms:description
      "[These findings indicate that mutations of the PPP2R1B gene are infrequent in ovarian cancer and that deletions affecting the distal portion of chromosome 11q in ovarian cancer likely target inactivation of other genes.]. 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:10935485;
    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:NP222186.RAcqYv4Gk7M3L-z4QotkTf6N1GWfH1qCs9NV3yduqUKdc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:03+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" .
}