@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP310864.RA_T5tc7SDlicDoAmb50g6W_bwYxzxB7HmCLPNUXEiFd4> .
@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:NP310864.RA_T5tc7SDlicDoAmb50g6W_bwYxzxB7HmCLPNUXEiFd4130_head {
  this: np:hasAssertion dgn-np:NP310864.RA_T5tc7SDlicDoAmb50g6W_bwYxzxB7HmCLPNUXEiFd4130_assertion;
    np:hasProvenance dgn-np:NP310864.RA_T5tc7SDlicDoAmb50g6W_bwYxzxB7HmCLPNUXEiFd4130_provenance;
    np:hasPublicationInfo dgn-np:NP310864.RA_T5tc7SDlicDoAmb50g6W_bwYxzxB7HmCLPNUXEiFd4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP310864.RA_T5tc7SDlicDoAmb50g6W_bwYxzxB7HmCLPNUXEiFd4130_assertion a np:Assertion .
  
  dgn-np:NP310864.RA_T5tc7SDlicDoAmb50g6W_bwYxzxB7HmCLPNUXEiFd4130_provenance a np:Provenance .
  
  dgn-np:NP310864.RA_T5tc7SDlicDoAmb50g6W_bwYxzxB7HmCLPNUXEiFd4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP310864.RA_T5tc7SDlicDoAmb50g6W_bwYxzxB7HmCLPNUXEiFd4130_assertion {
  miriam-gene:1111 a ncit:C16612 .
  
  lld:C0678222 a ncit:C7057 .
  
  dgn-gda:DGN45c2a0d4414951d9c7a7ea2e4e1121ce sio:SIO_000628 miriam-gene:1111, lld:C0678222;
    a sio:SIO_001121 .
}

dgn-np:NP310864.RA_T5tc7SDlicDoAmb50g6W_bwYxzxB7HmCLPNUXEiFd4130_provenance {
  dgn-np:NP310864.RA_T5tc7SDlicDoAmb50g6W_bwYxzxB7HmCLPNUXEiFd4130_assertion dcterms:description
      "[The cell cycle checkpoint kinase 2 (CHEK2) gene I157T variant may be associated with an increased risk of breast cancer, but it is unclear whether the evidence is sufficient to recommend testing for the mutation in clinical practice.]. 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:22799331;
    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:NP310864.RA_T5tc7SDlicDoAmb50g6W_bwYxzxB7HmCLPNUXEiFd4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:58+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" .
}