@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP687510.RA3TCTV795bO2Fqeo3MOAjTAEOwPwsDOtXH-e6RKxgriU> .
@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:NP687510.RA3TCTV795bO2Fqeo3MOAjTAEOwPwsDOtXH-e6RKxgriU130_head {
  this: np:hasAssertion dgn-np:NP687510.RA3TCTV795bO2Fqeo3MOAjTAEOwPwsDOtXH-e6RKxgriU130_assertion;
    np:hasProvenance dgn-np:NP687510.RA3TCTV795bO2Fqeo3MOAjTAEOwPwsDOtXH-e6RKxgriU130_provenance;
    np:hasPublicationInfo dgn-np:NP687510.RA3TCTV795bO2Fqeo3MOAjTAEOwPwsDOtXH-e6RKxgriU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP687510.RA3TCTV795bO2Fqeo3MOAjTAEOwPwsDOtXH-e6RKxgriU130_assertion a np:Assertion .
  
  dgn-np:NP687510.RA3TCTV795bO2Fqeo3MOAjTAEOwPwsDOtXH-e6RKxgriU130_provenance a np:Provenance .
  
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      np:PublicationInfo .
}

dgn-np:NP687510.RA3TCTV795bO2Fqeo3MOAjTAEOwPwsDOtXH-e6RKxgriU130_assertion {
  miriam-gene:3161 a ncit:C16612 .
  
  lld:C0678222 a ncit:C7057 .
  
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    a sio:SIO_001121 .
}

dgn-np:NP687510.RA3TCTV795bO2Fqeo3MOAjTAEOwPwsDOtXH-e6RKxgriU130_provenance {
  dgn-np:NP687510.RA3TCTV795bO2Fqeo3MOAjTAEOwPwsDOtXH-e6RKxgriU130_assertion dcterms:description
      "[We have examined the association of these single nucleotide polymorphisms, together with others tagging the HMMR gene, in a larger, European case-control study and find no association of any of them with risk of breast cancer: rs10515860 [odds ratio (OR; AA/GG), 0.85; 95% confidence interval (CI), 0.65-1.12; P(trend) = 0.9], rs299290 [OR (CC/TT), 1.00; 95% CI, 0.87-1.15; P(trend) = 0.7], rs3756648 (rs7712023) [OR (TT/CC), 0.93; 95% CI, 0.84-1.02; P(trend) = 0.1], rs299284 [OR (TT/CC), 1.01; 95% CI, 0.76-1.35; P(trend) = 0.5], and rs13183712 [OR (TT/GG), 1.04; 95% CI, 0.88-1.23; P(trend) = 0.6].]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
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  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:NP687510.RA3TCTV795bO2Fqeo3MOAjTAEOwPwsDOtXH-e6RKxgriU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:58+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
    dcterms:subject sio:SIO_000983;
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    pav:authoredBy <http://orcid.org/0000-0001-5999-6269>, <http://orcid.org/0000-0002-7534-7661>,
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    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
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