@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP745114.RATfQ1Nc5S7LOH9cru0UbpK_bTc6ibCWDAxF0L_PmO_kI> .
@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:NP745114.RATfQ1Nc5S7LOH9cru0UbpK_bTc6ibCWDAxF0L_PmO_kI130_head {
  this: np:hasAssertion dgn-np:NP745114.RATfQ1Nc5S7LOH9cru0UbpK_bTc6ibCWDAxF0L_PmO_kI130_assertion;
    np:hasProvenance dgn-np:NP745114.RATfQ1Nc5S7LOH9cru0UbpK_bTc6ibCWDAxF0L_PmO_kI130_provenance;
    np:hasPublicationInfo dgn-np:NP745114.RATfQ1Nc5S7LOH9cru0UbpK_bTc6ibCWDAxF0L_PmO_kI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP745114.RATfQ1Nc5S7LOH9cru0UbpK_bTc6ibCWDAxF0L_PmO_kI130_assertion a np:Assertion .
  
  dgn-np:NP745114.RATfQ1Nc5S7LOH9cru0UbpK_bTc6ibCWDAxF0L_PmO_kI130_provenance a np:Provenance .
  
  dgn-np:NP745114.RATfQ1Nc5S7LOH9cru0UbpK_bTc6ibCWDAxF0L_PmO_kI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP745114.RATfQ1Nc5S7LOH9cru0UbpK_bTc6ibCWDAxF0L_PmO_kI130_assertion {
  miriam-gene:8170 a ncit:C16612 .
  
  lld:C0023467 a ncit:C7057 .
  
  dgn-gda:DGN000c55561aeb3ef4a3efba312935c4b4 sio:SIO_000628 miriam-gene:8170, lld:C0023467;
    a sio:SIO_001121 .
}

dgn-np:NP745114.RATfQ1Nc5S7LOH9cru0UbpK_bTc6ibCWDAxF0L_PmO_kI130_provenance {
  dgn-np:NP745114.RATfQ1Nc5S7LOH9cru0UbpK_bTc6ibCWDAxF0L_PmO_kI130_assertion dcterms:description
      "[To investigate whether inherited variants in genes encoding proteins that repair DSBs by HR modulate acute myeloid leukaemia (AML) risk, we have examined the frequency of two variants in the 5' untranslated region (UTR) of RAD51 (RAD51 135 G>C and the RAD51 172 G>T) in a large case-control study of acute myeloid leukaemia (AML).]. 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:16890287;
    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:NP745114.RATfQ1Nc5S7LOH9cru0UbpK_bTc6ibCWDAxF0L_PmO_kI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:32+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" .
}