@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP544749.RAk6dClwrrZpeOtmRlIPEpHZIeyQmVFXMpgzn9fJ2Cylw> .
@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:NP544749.RAk6dClwrrZpeOtmRlIPEpHZIeyQmVFXMpgzn9fJ2Cylw130_head {
   this: np:hasAssertion dgn-np:NP544749.RAk6dClwrrZpeOtmRlIPEpHZIeyQmVFXMpgzn9fJ2Cylw130_assertion ;
    np:hasProvenance dgn-np:NP544749.RAk6dClwrrZpeOtmRlIPEpHZIeyQmVFXMpgzn9fJ2Cylw130_provenance ;
    np:hasPublicationInfo dgn-np:NP544749.RAk6dClwrrZpeOtmRlIPEpHZIeyQmVFXMpgzn9fJ2Cylw130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP544749.RAk6dClwrrZpeOtmRlIPEpHZIeyQmVFXMpgzn9fJ2Cylw130_assertion a np:Assertion .
  dgn-np:NP544749.RAk6dClwrrZpeOtmRlIPEpHZIeyQmVFXMpgzn9fJ2Cylw130_provenance a np:Provenance .
  dgn-np:NP544749.RAk6dClwrrZpeOtmRlIPEpHZIeyQmVFXMpgzn9fJ2Cylw130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP544749.RAk6dClwrrZpeOtmRlIPEpHZIeyQmVFXMpgzn9fJ2Cylw130_assertion {
   miriam-gene:2099 a ncit:C16612 .
  lld:C0007222 a ncit:C7057 .
  dgn-gda:DGNf4535746eff4151825774b6bb39350fc sio:SIO_000628 miriam-gene:2099 , lld:C0007222 ;
    a sio:SIO_001121 .
}
dgn-np:NP544749.RAk6dClwrrZpeOtmRlIPEpHZIeyQmVFXMpgzn9fJ2Cylw130_provenance {
   dgn-np:NP544749.RAk6dClwrrZpeOtmRlIPEpHZIeyQmVFXMpgzn9fJ2Cylw130_assertion dcterms:description "[The relation between ESR1 variation and CAD may influence clinical decisions such as the use of hormone therapy, and additionally will be helpful to identify the genetic susceptibility determinants of cardiovascular disease development.]. 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:16612467 ;
    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:NP544749.RAk6dClwrrZpeOtmRlIPEpHZIeyQmVFXMpgzn9fJ2Cylw130_publicationInfo {
   this: dcterms:created "2016-05-13T12:45:51+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> ;
    pav:version "v4.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}