@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1256498.RA9iLWi6IWVmVarlpNh-rLX7vxU7eUe1JJ3QUwM0VVHK4
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
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{
this:
np:hasAssertion
dgn-np:NP1256498.RA9iLWi6IWVmVarlpNh-rLX7vxU7eUe1JJ3QUwM0VVHK4130_assertion
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a
np:Nanopublication
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dgn-np:NP1256498.RA9iLWi6IWVmVarlpNh-rLX7vxU7eUe1JJ3QUwM0VVHK4130_assertion
a
np:Assertion
.
dgn-np:NP1256498.RA9iLWi6IWVmVarlpNh-rLX7vxU7eUe1JJ3QUwM0VVHK4130_provenance
a
np:Provenance
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{
miriam-gene:1312
a
ncit:C16612
.
lld:C0338480
a
ncit:C7057
.
dgn-gda:DGN9dec9c905115336af1f3087fac23b572
sio:SIO_000628
miriam-gene:1312
,
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;
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.
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dgn-np:NP1256498.RA9iLWi6IWVmVarlpNh-rLX7vxU7eUe1JJ3QUwM0VVHK4130_provenance
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dgn-np:NP1256498.RA9iLWi6IWVmVarlpNh-rLX7vxU7eUe1JJ3QUwM0VVHK4130_assertion
dcterms:description
"[Using T1-weighted and resting functional MRI, we evaluated the effect of COMT genetic variations on migraine and possible interactions between COMT and the disease in brain structure and function in 135 females with migraine without aura (MWoA) and 111 matched health controls (HC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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miriam-pubmed:25598522
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prov:wasDerivedFrom
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prov:wasGeneratedBy
eco:ECO_0000203
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dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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 .
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dgn-np:NP1256498.RA9iLWi6IWVmVarlpNh-rLX7vxU7eUe1JJ3QUwM0VVHK4130_publicationInfo
{
this:
dcterms:created
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xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
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prv:usedData
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pav:authoredBy
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> , <
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> , <
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> ;
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