@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP161805.RATPaNkkDkoTDDw2GRjBfviB7q7Bih1vfMqXlSAu9ttzM> .
@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:NP161805.RATPaNkkDkoTDDw2GRjBfviB7q7Bih1vfMqXlSAu9ttzM130_head {
   this: np:hasAssertion dgn-np:NP161805.RATPaNkkDkoTDDw2GRjBfviB7q7Bih1vfMqXlSAu9ttzM130_assertion ;
    np:hasProvenance dgn-np:NP161805.RATPaNkkDkoTDDw2GRjBfviB7q7Bih1vfMqXlSAu9ttzM130_provenance ;
    np:hasPublicationInfo dgn-np:NP161805.RATPaNkkDkoTDDw2GRjBfviB7q7Bih1vfMqXlSAu9ttzM130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP161805.RATPaNkkDkoTDDw2GRjBfviB7q7Bih1vfMqXlSAu9ttzM130_assertion a np:Assertion .
  dgn-np:NP161805.RATPaNkkDkoTDDw2GRjBfviB7q7Bih1vfMqXlSAu9ttzM130_provenance a np:Provenance .
  dgn-np:NP161805.RATPaNkkDkoTDDw2GRjBfviB7q7Bih1vfMqXlSAu9ttzM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP161805.RATPaNkkDkoTDDw2GRjBfviB7q7Bih1vfMqXlSAu9ttzM130_assertion {
   miriam-gene:8204 a ncit:C16612 .
  lld:C2678504 a ncit:C7057 .
  dgn-gda:DGN2df6aa007f52203226a3b1676d73f578 sio:SIO_000628 miriam-gene:8204 , lld:C2678504 ;
    a sio:SIO_001121 .
}
dgn-np:NP161805.RATPaNkkDkoTDDw2GRjBfviB7q7Bih1vfMqXlSAu9ttzM130_provenance {
   dgn-np:NP161805.RATPaNkkDkoTDDw2GRjBfviB7q7Bih1vfMqXlSAu9ttzM130_assertion dcterms:description "[Looking for markers related to osteoporosis, we have analyzed five single nucleotide polymorphisms located in genes related to the estrogen pathway, Follicle Stimulating Hormone Receptor (FSHR) gene, the CYP19 aromatase (CYP19A1) gene, the Estrogen Receptor alpha (ESR1) gene, the Estrogen Receptor beta (ESR2) gene and the Nuclear Receptor Interacting Protein 1 (NRIP1) gene in 265 unrelated postmenopausal women.]. 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:16530497 ;
    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:NP161805.RATPaNkkDkoTDDw2GRjBfviB7q7Bih1vfMqXlSAu9ttzM130_publicationInfo {
   this: dcterms:created "2014-10-02T12:33:27+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" .
}