@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP626776.RAXMxJyh_qPoOumnpyOkNT0yiwPkDGDhfMC3eVXfG8WY4> .
@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:NP626776.RAXMxJyh_qPoOumnpyOkNT0yiwPkDGDhfMC3eVXfG8WY4130_head {
  this: np:hasAssertion dgn-np:NP626776.RAXMxJyh_qPoOumnpyOkNT0yiwPkDGDhfMC3eVXfG8WY4130_assertion;
    np:hasProvenance dgn-np:NP626776.RAXMxJyh_qPoOumnpyOkNT0yiwPkDGDhfMC3eVXfG8WY4130_provenance;
    np:hasPublicationInfo dgn-np:NP626776.RAXMxJyh_qPoOumnpyOkNT0yiwPkDGDhfMC3eVXfG8WY4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP626776.RAXMxJyh_qPoOumnpyOkNT0yiwPkDGDhfMC3eVXfG8WY4130_assertion a np:Assertion .
  
  dgn-np:NP626776.RAXMxJyh_qPoOumnpyOkNT0yiwPkDGDhfMC3eVXfG8WY4130_provenance a np:Provenance .
  
  dgn-np:NP626776.RAXMxJyh_qPoOumnpyOkNT0yiwPkDGDhfMC3eVXfG8WY4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP626776.RAXMxJyh_qPoOumnpyOkNT0yiwPkDGDhfMC3eVXfG8WY4130_assertion {
  miriam-gene:11200 a ncit:C16612 .
  
  lld:C0678222 a ncit:C7057 .
  
  dgn-gda:DGN9eed41ef8312475b46f7b63562c18bea sio:SIO_000628 miriam-gene:11200, lld:C0678222;
    a sio:SIO_001122 .
}

dgn-np:NP626776.RAXMxJyh_qPoOumnpyOkNT0yiwPkDGDhfMC3eVXfG8WY4130_provenance {
  dgn-np:NP626776.RAXMxJyh_qPoOumnpyOkNT0yiwPkDGDhfMC3eVXfG8WY4130_assertion dcterms:description
      "[Our findings highlight the notion that clinical testing for rare missense mutations within CHEK2 may have limited value in predicting breast cancer risk, but that testing for the 1100delC variant may be valuable in phenotypically- and geographically-selected populations.]. 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:17721994;
    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:NP626776.RAXMxJyh_qPoOumnpyOkNT0yiwPkDGDhfMC3eVXfG8WY4130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:29+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" .
}