@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP732569.RAEDrMIiORjVBs8fmb058RxXupehdO3EUmQZ_YiPr6tfw> .
@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:NP732569.RAEDrMIiORjVBs8fmb058RxXupehdO3EUmQZ_YiPr6tfw130_head {
  this: np:hasAssertion dgn-np:NP732569.RAEDrMIiORjVBs8fmb058RxXupehdO3EUmQZ_YiPr6tfw130_assertion;
    np:hasProvenance dgn-np:NP732569.RAEDrMIiORjVBs8fmb058RxXupehdO3EUmQZ_YiPr6tfw130_provenance;
    np:hasPublicationInfo dgn-np:NP732569.RAEDrMIiORjVBs8fmb058RxXupehdO3EUmQZ_YiPr6tfw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP732569.RAEDrMIiORjVBs8fmb058RxXupehdO3EUmQZ_YiPr6tfw130_assertion a np:Assertion .
  
  dgn-np:NP732569.RAEDrMIiORjVBs8fmb058RxXupehdO3EUmQZ_YiPr6tfw130_provenance a np:Provenance .
  
  dgn-np:NP732569.RAEDrMIiORjVBs8fmb058RxXupehdO3EUmQZ_YiPr6tfw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP732569.RAEDrMIiORjVBs8fmb058RxXupehdO3EUmQZ_YiPr6tfw130_assertion {
  miriam-gene:26227 a ncit:C16612 .
  
  lld:C0376415 a ncit:C7057 .
  
  dgn-gda:DGNcad04cc6c9411f007057200be1f3f6d2 sio:SIO_000628 miriam-gene:26227, lld:C0376415;
    a sio:SIO_001121 .
}

dgn-np:NP732569.RAEDrMIiORjVBs8fmb058RxXupehdO3EUmQZ_YiPr6tfw130_provenance {
  dgn-np:NP732569.RAEDrMIiORjVBs8fmb058RxXupehdO3EUmQZ_YiPr6tfw130_assertion dcterms:description
      "[Preimplantation genetic diagnosis (PGD) has recently been performed for inherited cancer predisposition determined by p53 tumour suppressor gene mutations, suggesting the usefulness of PGD for late onset disorders with genetic predisposition, including those caused by the germline mutations of other tumour suppressor 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:12709270;
    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:NP732569.RAEDrMIiORjVBs8fmb058RxXupehdO3EUmQZ_YiPr6tfw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:24+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" .
}