@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP869424.RA8R7CynaHlE6er8fINzjbN8FQpgQs55wj8DAGwWkrJMY> .
@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:NP869424.RA8R7CynaHlE6er8fINzjbN8FQpgQs55wj8DAGwWkrJMY130_head {
  this: np:hasAssertion dgn-np:NP869424.RA8R7CynaHlE6er8fINzjbN8FQpgQs55wj8DAGwWkrJMY130_assertion;
    np:hasProvenance dgn-np:NP869424.RA8R7CynaHlE6er8fINzjbN8FQpgQs55wj8DAGwWkrJMY130_provenance;
    np:hasPublicationInfo dgn-np:NP869424.RA8R7CynaHlE6er8fINzjbN8FQpgQs55wj8DAGwWkrJMY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP869424.RA8R7CynaHlE6er8fINzjbN8FQpgQs55wj8DAGwWkrJMY130_assertion a np:Assertion .
  
  dgn-np:NP869424.RA8R7CynaHlE6er8fINzjbN8FQpgQs55wj8DAGwWkrJMY130_provenance a np:Provenance .
  
  dgn-np:NP869424.RA8R7CynaHlE6er8fINzjbN8FQpgQs55wj8DAGwWkrJMY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP869424.RA8R7CynaHlE6er8fINzjbN8FQpgQs55wj8DAGwWkrJMY130_assertion {
  miriam-gene:672 a ncit:C16612 .
  
  lld:C0006142 a ncit:C7057 .
  
  dgn-gda:DGN9e952efbce7a3c351d3cf08b33685437 sio:SIO_000628 miriam-gene:672, lld:C0006142;
    a sio:SIO_001121 .
}

dgn-np:NP869424.RA8R7CynaHlE6er8fINzjbN8FQpgQs55wj8DAGwWkrJMY130_provenance {
  dgn-np:NP869424.RA8R7CynaHlE6er8fINzjbN8FQpgQs55wj8DAGwWkrJMY130_assertion dcterms:description
      "[BRCA1 and BRCA2 mutation carriers could potentially be among the first groups of individuals for whom clinically applicable risk profiling could be developed using the common breast cancer susceptibility variants identified through GWAS.]. 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:21285145;
    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:NP869424.RA8R7CynaHlE6er8fINzjbN8FQpgQs55wj8DAGwWkrJMY130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:18+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" .
}