@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP344871.RAaUA6tAHNSJMQ94Z5f6k3eZ6bJwLRI-_vGzyDtvNRETQ
> .
@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:NP344871.RAaUA6tAHNSJMQ94Z5f6k3eZ6bJwLRI-_vGzyDtvNRETQ130_head
{
this:
np:hasAssertion
dgn-np:NP344871.RAaUA6tAHNSJMQ94Z5f6k3eZ6bJwLRI-_vGzyDtvNRETQ130_assertion
;
np:hasProvenance
dgn-np:NP344871.RAaUA6tAHNSJMQ94Z5f6k3eZ6bJwLRI-_vGzyDtvNRETQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP344871.RAaUA6tAHNSJMQ94Z5f6k3eZ6bJwLRI-_vGzyDtvNRETQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP344871.RAaUA6tAHNSJMQ94Z5f6k3eZ6bJwLRI-_vGzyDtvNRETQ130_assertion
a
np:Assertion
.
dgn-np:NP344871.RAaUA6tAHNSJMQ94Z5f6k3eZ6bJwLRI-_vGzyDtvNRETQ130_provenance
a
np:Provenance
.
dgn-np:NP344871.RAaUA6tAHNSJMQ94Z5f6k3eZ6bJwLRI-_vGzyDtvNRETQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP344871.RAaUA6tAHNSJMQ94Z5f6k3eZ6bJwLRI-_vGzyDtvNRETQ130_assertion
{
miriam-gene:1813
a
ncit:C16612
.
lld:C0149931
a
ncit:C7057
.
dgn-gda:DGN44411506e44fe9c6cd97651a29937ab5
sio:SIO_000628
miriam-gene:1813
,
lld:C0149931
;
a
sio:SIO_001121
.
}
dgn-np:NP344871.RAaUA6tAHNSJMQ94Z5f6k3eZ6bJwLRI-_vGzyDtvNRETQ130_provenance
{
dgn-np:NP344871.RAaUA6tAHNSJMQ94Z5f6k3eZ6bJwLRI-_vGzyDtvNRETQ130_assertion
dcterms:description
"[By multivariate logistic stepwise regression analysis, type of migraine, regular and sufficient dietary intake, and methylenetetrahydrofolate reductase (MTHFR) C677T (rs1801133) and dopamine D2 receptor (DRD2) C939T (rs6275) polymorphisms were selected as significant factors that contribute independently to the development from migraine to MOH (P < 0.05).]. 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:22290307
;
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:NP344871.RAaUA6tAHNSJMQ94Z5f6k3eZ6bJwLRI-_vGzyDtvNRETQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:22+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" .
}