@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP197171.RAiIyDQXKXdi_4i3d-He1YMMJ-GVGTBHZOPbSQXR6TM5o
> .
@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:NP197171.RAiIyDQXKXdi_4i3d-He1YMMJ-GVGTBHZOPbSQXR6TM5o130_head
{
this:
np:hasAssertion
dgn-np:NP197171.RAiIyDQXKXdi_4i3d-He1YMMJ-GVGTBHZOPbSQXR6TM5o130_assertion
;
np:hasProvenance
dgn-np:NP197171.RAiIyDQXKXdi_4i3d-He1YMMJ-GVGTBHZOPbSQXR6TM5o130_provenance
;
np:hasPublicationInfo
dgn-np:NP197171.RAiIyDQXKXdi_4i3d-He1YMMJ-GVGTBHZOPbSQXR6TM5o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP197171.RAiIyDQXKXdi_4i3d-He1YMMJ-GVGTBHZOPbSQXR6TM5o130_assertion
a
np:Assertion
.
dgn-np:NP197171.RAiIyDQXKXdi_4i3d-He1YMMJ-GVGTBHZOPbSQXR6TM5o130_provenance
a
np:Provenance
.
dgn-np:NP197171.RAiIyDQXKXdi_4i3d-He1YMMJ-GVGTBHZOPbSQXR6TM5o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP197171.RAiIyDQXKXdi_4i3d-He1YMMJ-GVGTBHZOPbSQXR6TM5o130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0154723
a
ncit:C7057
.
dgn-gda:DGNb32395c8e26874d7750870d73200b49b
sio:SIO_000628
miriam-gene:4524
,
lld:C0154723
;
a
sio:SIO_001121
.
}
dgn-np:NP197171.RAiIyDQXKXdi_4i3d-He1YMMJ-GVGTBHZOPbSQXR6TM5o130_provenance
{
dgn-np:NP197171.RAiIyDQXKXdi_4i3d-He1YMMJ-GVGTBHZOPbSQXR6TM5o130_assertion
dcterms:description
"[A first genotype-migraine association study was conducted on 100 patients with migraine with aura (MA), 106 with migraine without aura (MO), and 105 subjects without migraine, which provided evidence in favor of association of the TT677 MTHFR genotype with increased risk of MA compared with both control subjects (OR, 2.48; 95% CI, 1.11 to 5.58) and patients with MO (OR, 2.21; 95% CI, 1.01 to 4.82).]. 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:17962595
;
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:NP197171.RAiIyDQXKXdi_4i3d-He1YMMJ-GVGTBHZOPbSQXR6TM5o130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:48+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" .
}