@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP854483.RA_eIM90Pn2dCwJbCNZachYQ8fSUpABRIP1Xh0Blioka4> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP854483.RA_eIM90Pn2dCwJbCNZachYQ8fSUpABRIP1Xh0Blioka4130_head {
  this: np:hasAssertion dgn-np:NP854483.RA_eIM90Pn2dCwJbCNZachYQ8fSUpABRIP1Xh0Blioka4130_assertion;
    np:hasProvenance dgn-np:NP854483.RA_eIM90Pn2dCwJbCNZachYQ8fSUpABRIP1Xh0Blioka4130_provenance;
    np:hasPublicationInfo dgn-np:NP854483.RA_eIM90Pn2dCwJbCNZachYQ8fSUpABRIP1Xh0Blioka4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP854483.RA_eIM90Pn2dCwJbCNZachYQ8fSUpABRIP1Xh0Blioka4130_assertion a np:Assertion .
  
  dgn-np:NP854483.RA_eIM90Pn2dCwJbCNZachYQ8fSUpABRIP1Xh0Blioka4130_provenance a np:Provenance .
  
  dgn-np:NP854483.RA_eIM90Pn2dCwJbCNZachYQ8fSUpABRIP1Xh0Blioka4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP854483.RA_eIM90Pn2dCwJbCNZachYQ8fSUpABRIP1Xh0Blioka4130_assertion {
  miriam-gene:6462 a ncit:C16612 .
  
  lld:C0006142 a ncit:C7057 .
  
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dgn-np:NP854483.RA_eIM90Pn2dCwJbCNZachYQ8fSUpABRIP1Xh0Blioka4130_provenance {
  dgn-np:NP854483.RA_eIM90Pn2dCwJbCNZachYQ8fSUpABRIP1Xh0Blioka4130_assertion dcterms:description
      "[We hypothesized that heritable methylation potential might be a risk factor for breast cancer and evaluated possible association with breast cancer for single nucleotide polymorphisms (SNPs) either involving CpG sequences in extended 5'-regulatory regions of candidate genes (ESR1, ESR2, PGR, and SHBG) or CpG and missense coding SNPs in genes involved in methylation (MBD1, MECP2, DNMT1, MGMT, MTHFR, MTR, MTRR, MTHFD1, MTHFD2, BHMT, DCTD, and SLC19A1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
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    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP854483.RA_eIM90Pn2dCwJbCNZachYQ8fSUpABRIP1Xh0Blioka4130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:12+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
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