@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP156122.RA4jWGX-bMiz9WIjYJ1eOBkLF36tHFovGgos5-f4WzsfM> .
@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:NP156122.RA4jWGX-bMiz9WIjYJ1eOBkLF36tHFovGgos5-f4WzsfM130_head {
  this: np:hasAssertion dgn-np:NP156122.RA4jWGX-bMiz9WIjYJ1eOBkLF36tHFovGgos5-f4WzsfM130_assertion ;
    np:hasProvenance dgn-np:NP156122.RA4jWGX-bMiz9WIjYJ1eOBkLF36tHFovGgos5-f4WzsfM130_provenance ;
    np:hasPublicationInfo dgn-np:NP156122.RA4jWGX-bMiz9WIjYJ1eOBkLF36tHFovGgos5-f4WzsfM130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP156122.RA4jWGX-bMiz9WIjYJ1eOBkLF36tHFovGgos5-f4WzsfM130_assertion a np:Assertion .
  dgn-np:NP156122.RA4jWGX-bMiz9WIjYJ1eOBkLF36tHFovGgos5-f4WzsfM130_provenance a np:Provenance .
  dgn-np:NP156122.RA4jWGX-bMiz9WIjYJ1eOBkLF36tHFovGgos5-f4WzsfM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP156122.RA4jWGX-bMiz9WIjYJ1eOBkLF36tHFovGgos5-f4WzsfM130_assertion {
  miriam-gene:4810 a ncit:C16612 .
  lld:C0030567 a ncit:C7057 .
  dgn-gda:DGNc3be4b6276f6cc89b56196134ba992b4 sio:SIO_000628 miriam-gene:4810 , lld:C0030567 ;
    a sio:SIO_001121 .
}
dgn-np:NP156122.RA4jWGX-bMiz9WIjYJ1eOBkLF36tHFovGgos5-f4WzsfM130_provenance {
  dgn-np:NP156122.RA4jWGX-bMiz9WIjYJ1eOBkLF36tHFovGgos5-f4WzsfM130_assertion dcterms:description "[In a nested case-control study within the Nurses Health Study (NHS) and the Health Professionals Follow-up Study (HPFS), we examined associations between single nucleotide polymorphisms (SNPs) of caffeine metabolizing genes (CYP1A2 and NAT2) and estrogen receptors (ESR1 and ESR2), their interaction with caffeine intake and hormone replacement therapy (PMH) use (collected prospectively) and risk of PD.]. 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:20304699 ;
    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:NP156122.RA4jWGX-bMiz9WIjYJ1eOBkLF36tHFovGgos5-f4WzsfM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:24+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> ;
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}