@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP611684.RAxZwSCj0xOMJav6-eCtzzdu1LakiCtaAeBu-NXzqXb6E> .
@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:NP611684.RAxZwSCj0xOMJav6-eCtzzdu1LakiCtaAeBu-NXzqXb6E130_head {
  this: np:hasAssertion dgn-np:NP611684.RAxZwSCj0xOMJav6-eCtzzdu1LakiCtaAeBu-NXzqXb6E130_assertion;
    np:hasProvenance dgn-np:NP611684.RAxZwSCj0xOMJav6-eCtzzdu1LakiCtaAeBu-NXzqXb6E130_provenance;
    np:hasPublicationInfo dgn-np:NP611684.RAxZwSCj0xOMJav6-eCtzzdu1LakiCtaAeBu-NXzqXb6E130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP611684.RAxZwSCj0xOMJav6-eCtzzdu1LakiCtaAeBu-NXzqXb6E130_assertion a np:Assertion .
  
  dgn-np:NP611684.RAxZwSCj0xOMJav6-eCtzzdu1LakiCtaAeBu-NXzqXb6E130_provenance a np:Provenance .
  
  dgn-np:NP611684.RAxZwSCj0xOMJav6-eCtzzdu1LakiCtaAeBu-NXzqXb6E130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP611684.RAxZwSCj0xOMJav6-eCtzzdu1LakiCtaAeBu-NXzqXb6E130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  
  lld:C0277558 a ncit:C7057 .
  
  dgn-gda:DGN117e22c5ab5f9c36ff567f14ea2c65e7 sio:SIO_000628 miriam-gene:7157, lld:C0277558;
    a sio:SIO_001121 .
}

dgn-np:NP611684.RAxZwSCj0xOMJav6-eCtzzdu1LakiCtaAeBu-NXzqXb6E130_provenance {
  dgn-np:NP611684.RAxZwSCj0xOMJav6-eCtzzdu1LakiCtaAeBu-NXzqXb6E130_assertion dcterms:description
      "[In this study we investigated the role of the allelic variants in candidate genes acting in the tumor suppressor, DNA repair and p53 pathways as risk factors for familial breast cancer in 147 patients displaying characteristics of familial disease.]. 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:20358297;
    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:NP611684.RAxZwSCj0xOMJav6-eCtzzdu1LakiCtaAeBu-NXzqXb6E130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:10+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" .
}