@prefix dc: <
http://purl.org/dc/terms/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP96302.RAePdzqIGsPM_ppW3FYeJ2oXHflyEtNdy0mODteiwP4Zk
> .
@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 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:NP96302.RAePdzqIGsPM_ppW3FYeJ2oXHflyEtNdy0mODteiwP4Zk130_head
{
this:
np:hasAssertion
dgn-np:NP96302.RAePdzqIGsPM_ppW3FYeJ2oXHflyEtNdy0mODteiwP4Zk130_assertion
;
np:hasProvenance
dgn-np:NP96302.RAePdzqIGsPM_ppW3FYeJ2oXHflyEtNdy0mODteiwP4Zk130_provenance
;
np:hasPublicationInfo
dgn-np:NP96302.RAePdzqIGsPM_ppW3FYeJ2oXHflyEtNdy0mODteiwP4Zk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP96302.RAePdzqIGsPM_ppW3FYeJ2oXHflyEtNdy0mODteiwP4Zk130_assertion
a
np:Assertion
.
dgn-np:NP96302.RAePdzqIGsPM_ppW3FYeJ2oXHflyEtNdy0mODteiwP4Zk130_provenance
a
np:Provenance
.
dgn-np:NP96302.RAePdzqIGsPM_ppW3FYeJ2oXHflyEtNdy0mODteiwP4Zk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP96302.RAePdzqIGsPM_ppW3FYeJ2oXHflyEtNdy0mODteiwP4Zk130_assertion
{
miriam-gene:4188
a
ncit:C16612
.
lld:C0007222
a
ncit:C7057
.
dgn-gda:DGN580f91c563fce591f4cb330e78ba07f1
sio:SIO_000628
miriam-gene:4188
,
lld:C0007222
;
a
sio:SIO_001122
.
}
dgn-np:NP96302.RAePdzqIGsPM_ppW3FYeJ2oXHflyEtNdy0mODteiwP4Zk130_provenance
{
dgn-np:NP96302.RAePdzqIGsPM_ppW3FYeJ2oXHflyEtNdy0mODteiwP4Zk130_assertion
dc:description
"[Our results provide some suggestion for an association of five SNPs with CVD events among women with migraine; none of the results was genome-wide significant. Four associations appeared among migraineurs with aura, two of those with ischemic stroke. Although our population is among the largest with migraine and incident CVD information, these results must be treated with caution, given the limited number of CVD events among women with migraine and the low minor allele frequencies for three of the SNPs. Our results await independent replication and should be considered hypothesis generating for future research.]. 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:21779381
;
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:NP96302.RAePdzqIGsPM_ppW3FYeJ2oXHflyEtNdy0mODteiwP4Zk130_publicationInfo
{
this:
dc:created
"2014-10-02T12:32:48+02:00"^^
xsd:dateTime
;
dc:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dc:rightsHolder
dgn-void:IBIGroup
;
dc: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" .
}