@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP654308.RAxHBGLuobTdSDYSwxRDxrtV1nbOO4F-cJ5DiTZoAb1js> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP654308.RAxHBGLuobTdSDYSwxRDxrtV1nbOO4F-cJ5DiTZoAb1js130_head {
  this: np:hasAssertion dgn-np:NP654308.RAxHBGLuobTdSDYSwxRDxrtV1nbOO4F-cJ5DiTZoAb1js130_assertion;
    np:hasProvenance dgn-np:NP654308.RAxHBGLuobTdSDYSwxRDxrtV1nbOO4F-cJ5DiTZoAb1js130_provenance;
    np:hasPublicationInfo dgn-np:NP654308.RAxHBGLuobTdSDYSwxRDxrtV1nbOO4F-cJ5DiTZoAb1js130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP654308.RAxHBGLuobTdSDYSwxRDxrtV1nbOO4F-cJ5DiTZoAb1js130_assertion a np:Assertion .
  
  dgn-np:NP654308.RAxHBGLuobTdSDYSwxRDxrtV1nbOO4F-cJ5DiTZoAb1js130_provenance a np:Provenance .
  
  dgn-np:NP654308.RAxHBGLuobTdSDYSwxRDxrtV1nbOO4F-cJ5DiTZoAb1js130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP654308.RAxHBGLuobTdSDYSwxRDxrtV1nbOO4F-cJ5DiTZoAb1js130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  
  lld:C0006142 a ncit:C7057 .
  
  dgn-gda:DGN6635fce4bf65119bcced02e0ba10208c sio:SIO_000628 miriam-gene:7157, lld:C0006142;
    a sio:SIO_001121 .
}

dgn-np:NP654308.RAxHBGLuobTdSDYSwxRDxrtV1nbOO4F-cJ5DiTZoAb1js130_provenance {
  dgn-np:NP654308.RAxHBGLuobTdSDYSwxRDxrtV1nbOO4F-cJ5DiTZoAb1js130_assertion dcterms:description
      "[Mutations in genes such as TP53 and PTEN have also been linked with high risk for breast cancer within specific cancer syndromes and rare germline variants in genes such as CHEK2 and ATM have been found to confer modest risk to breast cancer.]. 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:18258506;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP654308.RAxHBGLuobTdSDYSwxRDxrtV1nbOO4F-cJ5DiTZoAb1js130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:41+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}