@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP784667.RAat6XsALhVJCf45nd99s7JBpsiedXv8PcvyG2xHNejUY> .
@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:NP784667.RAat6XsALhVJCf45nd99s7JBpsiedXv8PcvyG2xHNejUY130_head {
  this: np:hasAssertion dgn-np:NP784667.RAat6XsALhVJCf45nd99s7JBpsiedXv8PcvyG2xHNejUY130_assertion;
    np:hasProvenance dgn-np:NP784667.RAat6XsALhVJCf45nd99s7JBpsiedXv8PcvyG2xHNejUY130_provenance;
    np:hasPublicationInfo dgn-np:NP784667.RAat6XsALhVJCf45nd99s7JBpsiedXv8PcvyG2xHNejUY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP784667.RAat6XsALhVJCf45nd99s7JBpsiedXv8PcvyG2xHNejUY130_assertion a np:Assertion .
  
  dgn-np:NP784667.RAat6XsALhVJCf45nd99s7JBpsiedXv8PcvyG2xHNejUY130_provenance a np:Provenance .
  
  dgn-np:NP784667.RAat6XsALhVJCf45nd99s7JBpsiedXv8PcvyG2xHNejUY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP784667.RAat6XsALhVJCf45nd99s7JBpsiedXv8PcvyG2xHNejUY130_assertion {
  miriam-gene:3596 a ncit:C16612 .
  
  lld:C0006142 a ncit:C7057 .
  
  dgn-gda:DGNd409873c5a7158f82be34c9c2bc04a0b sio:SIO_000628 miriam-gene:3596, lld:C0006142;
    a sio:SIO_001121 .
}

dgn-np:NP784667.RAat6XsALhVJCf45nd99s7JBpsiedXv8PcvyG2xHNejUY130_provenance {
  dgn-np:NP784667.RAat6XsALhVJCf45nd99s7JBpsiedXv8PcvyG2xHNejUY130_assertion dcterms:description
      "[Despite observing no association between breast cancer and the single SNPs, results of this investigation suggest that the presence of CCA haplotype of IL13 gene may be associated with susceptibility of Iranian women to breast cancer.]. 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:18989750;
    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:NP784667.RAat6XsALhVJCf45nd99s7JBpsiedXv8PcvyG2xHNejUY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:55+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" .
}