@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP44750.RA35sjpeR2FpohYfC1u4R8GCCMlSZPKpkVnRj0ezvucm4
> .
@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:NP44750.RA35sjpeR2FpohYfC1u4R8GCCMlSZPKpkVnRj0ezvucm4130_head
{
this:
np:hasAssertion
dgn-np:NP44750.RA35sjpeR2FpohYfC1u4R8GCCMlSZPKpkVnRj0ezvucm4130_assertion
;
np:hasProvenance
dgn-np:NP44750.RA35sjpeR2FpohYfC1u4R8GCCMlSZPKpkVnRj0ezvucm4130_provenance
;
np:hasPublicationInfo
dgn-np:NP44750.RA35sjpeR2FpohYfC1u4R8GCCMlSZPKpkVnRj0ezvucm4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP44750.RA35sjpeR2FpohYfC1u4R8GCCMlSZPKpkVnRj0ezvucm4130_assertion
a
np:Assertion
.
dgn-np:NP44750.RA35sjpeR2FpohYfC1u4R8GCCMlSZPKpkVnRj0ezvucm4130_provenance
a
np:Provenance
.
dgn-np:NP44750.RA35sjpeR2FpohYfC1u4R8GCCMlSZPKpkVnRj0ezvucm4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP44750.RA35sjpeR2FpohYfC1u4R8GCCMlSZPKpkVnRj0ezvucm4130_assertion
{
miriam-gene:2099
a
ncit:C16612
.
lld:C0149931
a
ncit:C7057
.
dgn-gda:DGNac44835064634d7d6ab3c02c349406c0
sio:SIO_000628
miriam-gene:2099
,
lld:C0149931
;
a
sio:SIO_001122
.
}
dgn-np:NP44750.RA35sjpeR2FpohYfC1u4R8GCCMlSZPKpkVnRj0ezvucm4130_provenance
{
dgn-np:NP44750.RA35sjpeR2FpohYfC1u4R8GCCMlSZPKpkVnRj0ezvucm4130_assertion
dcterms:description
"[We aimed to explore the single-locus, haplotype and epistasis patterns and the contribution of oestrogen receptor ESR1 PvuII (rs2234693), ESR1 325 CG (rs1801132) and progesterone receptor PROGINS (rs1042838) polymorphisms in genetic susceptibility to migraine by analysing 613 subjects consisting of 217 migraine patients, 217 healthy controls (HC) and 179 patients with tension-type headache (TTH).]. 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:19673915
;
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:NP44750.RA35sjpeR2FpohYfC1u4R8GCCMlSZPKpkVnRj0ezvucm4130_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" .
}