@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP356557.RAh_dI1Gl4tsmj727E8W86txWfZivr97IjRJCVtZ3AMw8> .
@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:NP356557.RAh_dI1Gl4tsmj727E8W86txWfZivr97IjRJCVtZ3AMw8130_head {
  this: np:hasAssertion dgn-np:NP356557.RAh_dI1Gl4tsmj727E8W86txWfZivr97IjRJCVtZ3AMw8130_assertion ;
    np:hasProvenance dgn-np:NP356557.RAh_dI1Gl4tsmj727E8W86txWfZivr97IjRJCVtZ3AMw8130_provenance ;
    np:hasPublicationInfo dgn-np:NP356557.RAh_dI1Gl4tsmj727E8W86txWfZivr97IjRJCVtZ3AMw8130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP356557.RAh_dI1Gl4tsmj727E8W86txWfZivr97IjRJCVtZ3AMw8130_assertion a np:Assertion .
  dgn-np:NP356557.RAh_dI1Gl4tsmj727E8W86txWfZivr97IjRJCVtZ3AMw8130_provenance a np:Provenance .
  dgn-np:NP356557.RAh_dI1Gl4tsmj727E8W86txWfZivr97IjRJCVtZ3AMw8130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP356557.RAh_dI1Gl4tsmj727E8W86txWfZivr97IjRJCVtZ3AMw8130_assertion {
  miriam-gene:7439 a ncit:C16612 .
  lld:C0020538 a ncit:C7057 .
  dgn-gda:DGN84ff79b0002e6e1a9f496c7087fa7536 sio:SIO_000628 miriam-gene:7439 , lld:C0020538 ;
    a sio:SIO_001121 .
}
dgn-np:NP356557.RAh_dI1Gl4tsmj727E8W86txWfZivr97IjRJCVtZ3AMw8130_provenance {
  dgn-np:NP356557.RAh_dI1Gl4tsmj727E8W86txWfZivr97IjRJCVtZ3AMw8130_assertion dcterms:description "[Logistic regression analysis showed that the presence of Fx and of AH and the combination of the presence of Fx plus AH were associated with the H2 genotype regardless of the degree of cortisol secretion, age, BMI and BMD (OR 4.88, 95%CI 1.47-18.40, P = 0.05; OR 8.25, 95%CI 0.98-69.52, P = 0.05; OR 7.25, 95%CI 1.57-35.78, P = 0.011; respectively).]. 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:20584071 ;
    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:NP356557.RAh_dI1Gl4tsmj727E8W86txWfZivr97IjRJCVtZ3AMw8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:29+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" .
}