@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP889445.RARV4SNBZCnkj20XWPv2Mu0aIO-dwBND_KA2jdA6El-8g> .
@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:NP889445.RARV4SNBZCnkj20XWPv2Mu0aIO-dwBND_KA2jdA6El-8g130_head {
  this: np:hasAssertion dgn-np:NP889445.RARV4SNBZCnkj20XWPv2Mu0aIO-dwBND_KA2jdA6El-8g130_assertion;
    np:hasProvenance dgn-np:NP889445.RARV4SNBZCnkj20XWPv2Mu0aIO-dwBND_KA2jdA6El-8g130_provenance;
    np:hasPublicationInfo dgn-np:NP889445.RARV4SNBZCnkj20XWPv2Mu0aIO-dwBND_KA2jdA6El-8g130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP889445.RARV4SNBZCnkj20XWPv2Mu0aIO-dwBND_KA2jdA6El-8g130_assertion a np:Assertion .
  
  dgn-np:NP889445.RARV4SNBZCnkj20XWPv2Mu0aIO-dwBND_KA2jdA6El-8g130_provenance a np:Provenance .
  
  dgn-np:NP889445.RARV4SNBZCnkj20XWPv2Mu0aIO-dwBND_KA2jdA6El-8g130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP889445.RARV4SNBZCnkj20XWPv2Mu0aIO-dwBND_KA2jdA6El-8g130_assertion {
  miriam-gene:27324 a ncit:C16612 .
  
  lld:C0153690 a ncit:C7057 .
  
  dgn-gda:DGN46b5568a6e83f59b8e28f5c5fd0f5c29 sio:SIO_000628 miriam-gene:27324, lld:C0153690;
    a sio:SIO_001122 .
}

dgn-np:NP889445.RARV4SNBZCnkj20XWPv2Mu0aIO-dwBND_KA2jdA6El-8g130_provenance {
  dgn-np:NP889445.RARV4SNBZCnkj20XWPv2Mu0aIO-dwBND_KA2jdA6El-8g130_assertion dcterms:description
      "[rs3803662 of TNRC9 gene has been shown to be the SNP with the strongest association with BC, in particular, this polymorphism seems to be correlated with bone metastases and estrogen receptor positivity.]. 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:21996731;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP889445.RARV4SNBZCnkj20XWPv2Mu0aIO-dwBND_KA2jdA6El-8g130_publicationInfo {
  this: dcterms:created "2015-08-25T14:46:42+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" .
}