@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP286949.RAXltsHHeIAQYc1eFNlakT37WaF1KfJxyZooGirDY2OnY> .
@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:NP286949.RAXltsHHeIAQYc1eFNlakT37WaF1KfJxyZooGirDY2OnY130_head {
   this: np:hasAssertion dgn-np:NP286949.RAXltsHHeIAQYc1eFNlakT37WaF1KfJxyZooGirDY2OnY130_assertion ;
    np:hasProvenance dgn-np:NP286949.RAXltsHHeIAQYc1eFNlakT37WaF1KfJxyZooGirDY2OnY130_provenance ;
    np:hasPublicationInfo dgn-np:NP286949.RAXltsHHeIAQYc1eFNlakT37WaF1KfJxyZooGirDY2OnY130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP286949.RAXltsHHeIAQYc1eFNlakT37WaF1KfJxyZooGirDY2OnY130_assertion a np:Assertion .
  dgn-np:NP286949.RAXltsHHeIAQYc1eFNlakT37WaF1KfJxyZooGirDY2OnY130_provenance a np:Provenance .
  dgn-np:NP286949.RAXltsHHeIAQYc1eFNlakT37WaF1KfJxyZooGirDY2OnY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP286949.RAXltsHHeIAQYc1eFNlakT37WaF1KfJxyZooGirDY2OnY130_assertion {
   miriam-gene:2099 a ncit:C16612 .
  lld:C0242339 a ncit:C7057 .
  dgn-gda:DGN2118afd156cd5268182e779d21c90fb5 sio:SIO_000628 miriam-gene:2099 , lld:C0242339 ;
    a sio:SIO_001121 .
}
dgn-np:NP286949.RAXltsHHeIAQYc1eFNlakT37WaF1KfJxyZooGirDY2OnY130_provenance {
   dgn-np:NP286949.RAXltsHHeIAQYc1eFNlakT37WaF1KfJxyZooGirDY2OnY130_assertion dcterms:description "[To investigate genetic single nucleotide polymorphisms (SNPs) in estrogen receptor-α (ERα) (ESR1, rs2234693, rs1801132, rs7757956 and rs2813544) and ERβ (ESR2, rs3020450, rs7154455 and rs4986938) genes and relate them to the adverse effects lipodystrophy, dyslipidemia and metabolic syndrome as well as to differences in their prevalence between sexes in HIV-infected individuals on HAART.]. 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:22011627 ;
    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:NP286949.RAXltsHHeIAQYc1eFNlakT37WaF1KfJxyZooGirDY2OnY130_publicationInfo {
   this: dcterms:created "2014-10-02T12:34:43+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" .
}