@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP585927.RAMolHAjfDXgJST6the6nL9LcnelAZtmMzCCgyANwxCkk> .
@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:NP585927.RAMolHAjfDXgJST6the6nL9LcnelAZtmMzCCgyANwxCkk130_head {
  this: np:hasAssertion dgn-np:NP585927.RAMolHAjfDXgJST6the6nL9LcnelAZtmMzCCgyANwxCkk130_assertion;
    np:hasProvenance dgn-np:NP585927.RAMolHAjfDXgJST6the6nL9LcnelAZtmMzCCgyANwxCkk130_provenance;
    np:hasPublicationInfo dgn-np:NP585927.RAMolHAjfDXgJST6the6nL9LcnelAZtmMzCCgyANwxCkk130_publicationInfo;
    a np:Nanopublication .
  
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  dgn-np:NP585927.RAMolHAjfDXgJST6the6nL9LcnelAZtmMzCCgyANwxCkk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP585927.RAMolHAjfDXgJST6the6nL9LcnelAZtmMzCCgyANwxCkk130_assertion {
  miriam-gene:841 a ncit:C16612 .
  
  lld:C0029925 a ncit:C7057 .
  
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dgn-np:NP585927.RAMolHAjfDXgJST6the6nL9LcnelAZtmMzCCgyANwxCkk130_provenance {
  dgn-np:NP585927.RAMolHAjfDXgJST6the6nL9LcnelAZtmMzCCgyANwxCkk130_assertion dcterms:description
      "[The aim of the study is to investigate the relevance of rs1056663 and rs2708861 HUS1 polymorphisms, and rs104548, rs2981582 and rs2910164 polymorphisms of CASP8, FGFR2 and micro RNA 146A genes, respectively, as risk modifiers in hereditary breast or ovarian cancer (BC/OC) and risk factors in sporadic BC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
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    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;
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dgn-np:NP585927.RAMolHAjfDXgJST6the6nL9LcnelAZtmMzCCgyANwxCkk130_publicationInfo {
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    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
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    prv:usedData dgn-void:disgenetrdf;
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