@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP181074.RAhSSniJFBfEUCxzXlta9V9Iai2ekNE_VFjyqvwokqzI8> .
@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:NP181074.RAhSSniJFBfEUCxzXlta9V9Iai2ekNE_VFjyqvwokqzI8130_head {
  this: np:hasAssertion dgn-np:NP181074.RAhSSniJFBfEUCxzXlta9V9Iai2ekNE_VFjyqvwokqzI8130_assertion;
    np:hasProvenance dgn-np:NP181074.RAhSSniJFBfEUCxzXlta9V9Iai2ekNE_VFjyqvwokqzI8130_provenance;
    np:hasPublicationInfo dgn-np:NP181074.RAhSSniJFBfEUCxzXlta9V9Iai2ekNE_VFjyqvwokqzI8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP181074.RAhSSniJFBfEUCxzXlta9V9Iai2ekNE_VFjyqvwokqzI8130_assertion a np:Assertion .
  
  dgn-np:NP181074.RAhSSniJFBfEUCxzXlta9V9Iai2ekNE_VFjyqvwokqzI8130_provenance a np:Provenance .
  
  dgn-np:NP181074.RAhSSniJFBfEUCxzXlta9V9Iai2ekNE_VFjyqvwokqzI8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP181074.RAhSSniJFBfEUCxzXlta9V9Iai2ekNE_VFjyqvwokqzI8130_assertion {
  miriam-gene:2837 a ncit:C16612 .
  
  lld:C0678222 a ncit:C7057 .
  
  dgn-gda:DGNe17011cba2145a14e0b4af589b01a346 sio:SIO_000628 miriam-gene:2837, lld:C0678222;
    a sio:SIO_001121 .
}

dgn-np:NP181074.RAhSSniJFBfEUCxzXlta9V9Iai2ekNE_VFjyqvwokqzI8130_provenance {
  dgn-np:NP181074.RAhSSniJFBfEUCxzXlta9V9Iai2ekNE_VFjyqvwokqzI8130_assertion dcterms:description
      "[We examined the frequency of the 5'-untranslated region (5'-UTR) variant -77T-->C (rs 3213235) in 247 French breast cancer (BC) patients, 66 of whom were adverse radiotherapy responders, and 380 controls and determined the haplotypes based on this and the previously genotyped variants Arg194Trp, Arg280His and Arg399Gln.]. 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:16829685;
    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;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}

dgn-np:NP181074.RAhSSniJFBfEUCxzXlta9V9Iai2ekNE_VFjyqvwokqzI8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:38+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:disgenetrdf;
    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 "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}