@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1262335.RAsSibThrfCs09qb-nGfxPrGPeDt2Rzkn2C_6Zk-Gy134
> .
@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/
> .
dgn-np:NP1262335.RAsSibThrfCs09qb-nGfxPrGPeDt2Rzkn2C_6Zk-Gy134130_head
{
this:
np:hasAssertion
dgn-np:NP1262335.RAsSibThrfCs09qb-nGfxPrGPeDt2Rzkn2C_6Zk-Gy134130_assertion
;
np:hasProvenance
dgn-np:NP1262335.RAsSibThrfCs09qb-nGfxPrGPeDt2Rzkn2C_6Zk-Gy134130_provenance
;
np:hasPublicationInfo
dgn-np:NP1262335.RAsSibThrfCs09qb-nGfxPrGPeDt2Rzkn2C_6Zk-Gy134130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1262335.RAsSibThrfCs09qb-nGfxPrGPeDt2Rzkn2C_6Zk-Gy134130_assertion
a
np:Assertion
.
dgn-np:NP1262335.RAsSibThrfCs09qb-nGfxPrGPeDt2Rzkn2C_6Zk-Gy134130_provenance
a
np:Provenance
.
dgn-np:NP1262335.RAsSibThrfCs09qb-nGfxPrGPeDt2Rzkn2C_6Zk-Gy134130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1262335.RAsSibThrfCs09qb-nGfxPrGPeDt2Rzkn2C_6Zk-Gy134130_assertion
{
miriam-gene:57556
a
ncit:C16612
.
lld:C0751122
a
ncit:C7057
.
dgn-gda:DGN31d7c8445f57c2a0e7442d5121312fca
sio:SIO_000628
miriam-gene:57556
,
lld:C0751122
;
a
sio:SIO_001121
.
}
dgn-np:NP1262335.RAsSibThrfCs09qb-nGfxPrGPeDt2Rzkn2C_6Zk-Gy134130_provenance
{
dgn-np:NP1262335.RAsSibThrfCs09qb-nGfxPrGPeDt2Rzkn2C_6Zk-Gy134130_assertion
dcterms:description
"[With the arrival of new clinical trials for Dravet syndrome, we sought to determine the characteristics of the patient population with Dravet syndrome in Europe today, which has possibly evolved subsequent to the approval of stiripentol and the ability to diagnose milder clinical cases via genetic testing.]. 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:25666511
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
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 .
}
dgn-np:NP1262335.RAsSibThrfCs09qb-nGfxPrGPeDt2Rzkn2C_6Zk-Gy134130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:18+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
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;
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
"v4.0.0.0" .
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pav:version
"v4.0.0" .
}