@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP854485.RAB13x81-oC44PavwSQyY3li2DtXc68Q34gvmUfT1Qdas> .
@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:NP854485.RAB13x81-oC44PavwSQyY3li2DtXc68Q34gvmUfT1Qdas130_head {
   this: np:hasAssertion dgn-np:NP854485.RAB13x81-oC44PavwSQyY3li2DtXc68Q34gvmUfT1Qdas130_assertion ;
    np:hasProvenance dgn-np:NP854485.RAB13x81-oC44PavwSQyY3li2DtXc68Q34gvmUfT1Qdas130_provenance ;
    np:hasPublicationInfo dgn-np:NP854485.RAB13x81-oC44PavwSQyY3li2DtXc68Q34gvmUfT1Qdas130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP854485.RAB13x81-oC44PavwSQyY3li2DtXc68Q34gvmUfT1Qdas130_assertion a np:Assertion .
  dgn-np:NP854485.RAB13x81-oC44PavwSQyY3li2DtXc68Q34gvmUfT1Qdas130_provenance a np:Provenance .
  dgn-np:NP854485.RAB13x81-oC44PavwSQyY3li2DtXc68Q34gvmUfT1Qdas130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP854485.RAB13x81-oC44PavwSQyY3li2DtXc68Q34gvmUfT1Qdas130_assertion {
   miriam-gene:4552 a ncit:C16612 .
  lld:C0678222 a ncit:C7057 .
  dgn-gda:DGNa4e2e8591739683f487774aa59ba6589 sio:SIO_000628 miriam-gene:4552 , lld:C0678222 ;
    a sio:SIO_001121 .
}
dgn-np:NP854485.RAB13x81-oC44PavwSQyY3li2DtXc68Q34gvmUfT1Qdas130_provenance {
   dgn-np:NP854485.RAB13x81-oC44PavwSQyY3li2DtXc68Q34gvmUfT1Qdas130_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 ;
    wi:evidence dgn-void:source_evidence_literature ;
    sio:SIO_000772 miriam-pubmed:21105050 ;
    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:NP854485.RAB13x81-oC44PavwSQyY3li2DtXc68Q34gvmUfT1Qdas130_publicationInfo {
   this: dcterms:created "2016-05-13T12:48:12+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:disgenetv3.0rdf ;
    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> ;
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}