@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP44771.RA1oFpupAMwB8VGvATOoMlSMsIgnaVJDn3G4S-FueChEo> .
@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:NP44771.RA1oFpupAMwB8VGvATOoMlSMsIgnaVJDn3G4S-FueChEo130_head {
  this: np:hasAssertion dgn-np:NP44771.RA1oFpupAMwB8VGvATOoMlSMsIgnaVJDn3G4S-FueChEo130_assertion ;
    np:hasProvenance dgn-np:NP44771.RA1oFpupAMwB8VGvATOoMlSMsIgnaVJDn3G4S-FueChEo130_provenance ;
    np:hasPublicationInfo dgn-np:NP44771.RA1oFpupAMwB8VGvATOoMlSMsIgnaVJDn3G4S-FueChEo130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP44771.RA1oFpupAMwB8VGvATOoMlSMsIgnaVJDn3G4S-FueChEo130_assertion a np:Assertion .
  dgn-np:NP44771.RA1oFpupAMwB8VGvATOoMlSMsIgnaVJDn3G4S-FueChEo130_provenance a np:Provenance .
  dgn-np:NP44771.RA1oFpupAMwB8VGvATOoMlSMsIgnaVJDn3G4S-FueChEo130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP44771.RA1oFpupAMwB8VGvATOoMlSMsIgnaVJDn3G4S-FueChEo130_assertion {
  miriam-gene:2099 a ncit:C16612 .
  lld:C0497327 a ncit:C7057 .
  dgn-gda:DGN0eee343a1293ea6dbd0b68080d879f77 sio:SIO_000628 miriam-gene:2099 , lld:C0497327 ;
    a sio:SIO_001122 .
}
dgn-np:NP44771.RA1oFpupAMwB8VGvATOoMlSMsIgnaVJDn3G4S-FueChEo130_provenance {
  dgn-np:NP44771.RA1oFpupAMwB8VGvATOoMlSMsIgnaVJDn3G4S-FueChEo130_assertion dcterms:description "[ The distribution of ER polymorphisms was significantly different between Chinese and some other ethnic populations. The results suggested that ER-alpha gene polymorphisms might be related to the individual susceptibility to AD, especially in the females. However, it did not support the association of Ahr gene polymorphism with higher risk of senile dementia.]. 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:12852830 ;
    prov:wasDerivedFrom dgn-void:gad-20130706 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP44771.RA1oFpupAMwB8VGvATOoMlSMsIgnaVJDn3G4S-FueChEo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:20+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" .
}