@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
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}