@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP921688.RAjEooNcUP7tKrcOzo_6BLfPcHnQc_bm7IKhxq1TN0zdA
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP921688.RAjEooNcUP7tKrcOzo_6BLfPcHnQc_bm7IKhxq1TN0zdA130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP921688.RAjEooNcUP7tKrcOzo_6BLfPcHnQc_bm7IKhxq1TN0zdA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP921688.RAjEooNcUP7tKrcOzo_6BLfPcHnQc_bm7IKhxq1TN0zdA130_assertion
a
np:Assertion
.
dgn-np:NP921688.RAjEooNcUP7tKrcOzo_6BLfPcHnQc_bm7IKhxq1TN0zdA130_provenance
a
np:Provenance
.
dgn-np:NP921688.RAjEooNcUP7tKrcOzo_6BLfPcHnQc_bm7IKhxq1TN0zdA130_publicationInfo
a
np:PublicationInfo
.
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{
miriam-gene:6323
a
ncit:C16612
.
lld:C0014547
a
ncit:C7057
.
dgn-gda:DGNd8ce55e7753bb4a732adbcc59d11d2da
sio:SIO_000628
miriam-gene:6323
,
lld:C0014547
;
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.
}
dgn-np:NP921688.RAjEooNcUP7tKrcOzo_6BLfPcHnQc_bm7IKhxq1TN0zdA130_provenance
{
dgn-np:NP921688.RAjEooNcUP7tKrcOzo_6BLfPcHnQc_bm7IKhxq1TN0zdA130_assertion
dcterms:description
"[The results of the present study indicate that the rs3812718 SNP in the SCN1A gene is significantly associated with the retention rate of CBZ monotherapy in Chinese Han patients with focal epilepsy.]. 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:22292851
;
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 .
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dgn-np:NP921688.RAjEooNcUP7tKrcOzo_6BLfPcHnQc_bm7IKhxq1TN0zdA130_publicationInfo
{
this:
dcterms:created
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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
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pav:authoredBy
<
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> , <
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> , <
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
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"v2.1.0" .
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