@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP156713.RAYCQLq0Dd370AduuTpijRIjEVYV8vyFHHM_8tGu9F2-I> .
@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:NP156713.RAYCQLq0Dd370AduuTpijRIjEVYV8vyFHHM_8tGu9F2-I130_head {
  this: np:hasAssertion dgn-np:NP156713.RAYCQLq0Dd370AduuTpijRIjEVYV8vyFHHM_8tGu9F2-I130_assertion;
    np:hasProvenance dgn-np:NP156713.RAYCQLq0Dd370AduuTpijRIjEVYV8vyFHHM_8tGu9F2-I130_provenance;
    np:hasPublicationInfo dgn-np:NP156713.RAYCQLq0Dd370AduuTpijRIjEVYV8vyFHHM_8tGu9F2-I130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP156713.RAYCQLq0Dd370AduuTpijRIjEVYV8vyFHHM_8tGu9F2-I130_assertion a np:Assertion .
  
  dgn-np:NP156713.RAYCQLq0Dd370AduuTpijRIjEVYV8vyFHHM_8tGu9F2-I130_provenance a np:Provenance .
  
  dgn-np:NP156713.RAYCQLq0Dd370AduuTpijRIjEVYV8vyFHHM_8tGu9F2-I130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP156713.RAYCQLq0Dd370AduuTpijRIjEVYV8vyFHHM_8tGu9F2-I130_assertion {
  miriam-gene:7248 a ncit:C16612 .
  
  lld:C0004135 a ncit:C7057 .
  
  dgn-gda:DGN4b32462060ef40bf207ad67663596739 sio:SIO_000628 miriam-gene:7248, lld:C0004135;
    a sio:SIO_001121 .
}

dgn-np:NP156713.RAYCQLq0Dd370AduuTpijRIjEVYV8vyFHHM_8tGu9F2-I130_provenance {
  dgn-np:NP156713.RAYCQLq0Dd370AduuTpijRIjEVYV8vyFHHM_8tGu9F2-I130_assertion dcterms:description
      "[The fact that women carriers of ATM mutations can have an increased risk of developing breast cancer and that many sporadic breast tumours have reduced levels of the ATM protein broadens the scope of ATM's tumour suppressor within the breast.]. 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:12196249;
    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:NP156713.RAYCQLq0Dd370AduuTpijRIjEVYV8vyFHHM_8tGu9F2-I130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:24+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" .
}