@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP57945.RAICx-j9B9CuDobB9pWWTg0uR4RkAQN_8dQ_mtI9net84> .
@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/v3.0.0/void/> .

dgn-np:NP57945.RAICx-j9B9CuDobB9pWWTg0uR4RkAQN_8dQ_mtI9net84130_head {
  this: np:hasAssertion dgn-np:NP57945.RAICx-j9B9CuDobB9pWWTg0uR4RkAQN_8dQ_mtI9net84130_assertion;
    np:hasProvenance dgn-np:NP57945.RAICx-j9B9CuDobB9pWWTg0uR4RkAQN_8dQ_mtI9net84130_provenance;
    np:hasPublicationInfo dgn-np:NP57945.RAICx-j9B9CuDobB9pWWTg0uR4RkAQN_8dQ_mtI9net84130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP57945.RAICx-j9B9CuDobB9pWWTg0uR4RkAQN_8dQ_mtI9net84130_assertion a np:Assertion .
  
  dgn-np:NP57945.RAICx-j9B9CuDobB9pWWTg0uR4RkAQN_8dQ_mtI9net84130_provenance a np:Provenance .
  
  dgn-np:NP57945.RAICx-j9B9CuDobB9pWWTg0uR4RkAQN_8dQ_mtI9net84130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP57945.RAICx-j9B9CuDobB9pWWTg0uR4RkAQN_8dQ_mtI9net84130_assertion {
  miriam-gene:675 a ncit:C16612 .
  
  lld:C0006142 a ncit:C7057 .
  
  dgn-gda:DGN3a00e980353dbae5c0c5014f5f6f3f1f sio:SIO_000628 miriam-gene:675, lld:C0006142;
    a sio:SIO_001122 .
}

dgn-np:NP57945.RAICx-j9B9CuDobB9pWWTg0uR4RkAQN_8dQ_mtI9net84130_provenance {
  dgn-np:NP57945.RAICx-j9B9CuDobB9pWWTg0uR4RkAQN_8dQ_mtI9net84130_assertion dcterms:description
      "[The founder mutation, BRCA1 3171ins5, explains the excess of ovarian cancer after breast cancer in the region. From the relative frequency of the studied mutations found at the cancer genetic counselling clinic, it is estimated that BRCA1 gene mutations a]. 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:20151938;
    prov:wasDerivedFrom dgn-void:gad-20150221;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP57945.RAICx-j9B9CuDobB9pWWTg0uR4RkAQN_8dQ_mtI9net84130_publicationInfo {
  this: dcterms:created "2015-08-25T14:38:11+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}