@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP489941.RAJp4cG2QIcQawsDvC656KQbYqN9eLB50bxVBnGZARH30> .
@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:NP489941.RAJp4cG2QIcQawsDvC656KQbYqN9eLB50bxVBnGZARH30130_head {
   this: np:hasAssertion dgn-np:NP489941.RAJp4cG2QIcQawsDvC656KQbYqN9eLB50bxVBnGZARH30130_assertion ;
    np:hasProvenance dgn-np:NP489941.RAJp4cG2QIcQawsDvC656KQbYqN9eLB50bxVBnGZARH30130_provenance ;
    np:hasPublicationInfo dgn-np:NP489941.RAJp4cG2QIcQawsDvC656KQbYqN9eLB50bxVBnGZARH30130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP489941.RAJp4cG2QIcQawsDvC656KQbYqN9eLB50bxVBnGZARH30130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP489941.RAJp4cG2QIcQawsDvC656KQbYqN9eLB50bxVBnGZARH30130_assertion {
   miriam-gene:84464 a ncit:C16612 .
  lld:C0346153 a ncit:C7057 .
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    a sio:SIO_001121 .
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dgn-np:NP489941.RAJp4cG2QIcQawsDvC656KQbYqN9eLB50bxVBnGZARH30130_provenance {
   dgn-np:NP489941.RAJp4cG2QIcQawsDvC656KQbYqN9eLB50bxVBnGZARH30130_assertion dcterms:description "[To investigate whether monoallelic SLX4 gene defects play some role in the inherited component of breast cancer susceptibility, in this study we resequenced the whole SLX4 coding region and flanking untranslated sections in genomic DNA samples obtained from a total of 52 German or Byelorussian patients with familial breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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    prov:wasDerivedFrom dgn-void:befree-20140225 ;
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    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
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dgn-np:NP489941.RAJp4cG2QIcQawsDvC656KQbYqN9eLB50bxVBnGZARH30130_publicationInfo {
   this: dcterms:created "2014-10-02T12:36:52+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
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