@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP375887.RAKwn28GYM2eP8eXQ-gcIWYtozIZPbpRyLmJgxu0IvBg8> .
@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:NP375887.RAKwn28GYM2eP8eXQ-gcIWYtozIZPbpRyLmJgxu0IvBg8130_head {
  this: np:hasAssertion dgn-np:NP375887.RAKwn28GYM2eP8eXQ-gcIWYtozIZPbpRyLmJgxu0IvBg8130_assertion;
    np:hasProvenance dgn-np:NP375887.RAKwn28GYM2eP8eXQ-gcIWYtozIZPbpRyLmJgxu0IvBg8130_provenance;
    np:hasPublicationInfo dgn-np:NP375887.RAKwn28GYM2eP8eXQ-gcIWYtozIZPbpRyLmJgxu0IvBg8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP375887.RAKwn28GYM2eP8eXQ-gcIWYtozIZPbpRyLmJgxu0IvBg8130_assertion a np:Assertion .
  
  dgn-np:NP375887.RAKwn28GYM2eP8eXQ-gcIWYtozIZPbpRyLmJgxu0IvBg8130_provenance a np:Provenance .
  
  dgn-np:NP375887.RAKwn28GYM2eP8eXQ-gcIWYtozIZPbpRyLmJgxu0IvBg8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP375887.RAKwn28GYM2eP8eXQ-gcIWYtozIZPbpRyLmJgxu0IvBg8130_assertion {
  miriam-gene:11200 a ncit:C16612 .
  
  lld:C0596263 a ncit:C7057 .
  
  dgn-gda:DGN787b77819d61430ec6b8c0f896ad8cb0 sio:SIO_000628 miriam-gene:11200, lld:C0596263;
    a sio:SIO_001122 .
}

dgn-np:NP375887.RAKwn28GYM2eP8eXQ-gcIWYtozIZPbpRyLmJgxu0IvBg8130_provenance {
  dgn-np:NP375887.RAKwn28GYM2eP8eXQ-gcIWYtozIZPbpRyLmJgxu0IvBg8130_assertion dcterms:description
      "[This study provides further evidence that sequence variation in CHEK2 is associated with an increased risk of breast cancer, and implies that tumorigenesis in association with CHEK2 mutations does not involve loss of the wild type allele.]. 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:12454775;
    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:NP375887.RAKwn28GYM2eP8eXQ-gcIWYtozIZPbpRyLmJgxu0IvBg8130_publicationInfo {
  this: dcterms:created "2016-05-13T12:44:35+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" .
}