@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP461849.RArdOi_tqaVeBAGFnbu9NR66bK1AcMLn7GHgpIYpKDLKs
> .
@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:NP461849.RArdOi_tqaVeBAGFnbu9NR66bK1AcMLn7GHgpIYpKDLKs130_assertion
;
np:hasProvenance
dgn-np:NP461849.RArdOi_tqaVeBAGFnbu9NR66bK1AcMLn7GHgpIYpKDLKs130_provenance
;
np:hasPublicationInfo
dgn-np:NP461849.RArdOi_tqaVeBAGFnbu9NR66bK1AcMLn7GHgpIYpKDLKs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP461849.RArdOi_tqaVeBAGFnbu9NR66bK1AcMLn7GHgpIYpKDLKs130_assertion
a
np:Assertion
.
dgn-np:NP461849.RArdOi_tqaVeBAGFnbu9NR66bK1AcMLn7GHgpIYpKDLKs130_provenance
a
np:Provenance
.
dgn-np:NP461849.RArdOi_tqaVeBAGFnbu9NR66bK1AcMLn7GHgpIYpKDLKs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP461849.RArdOi_tqaVeBAGFnbu9NR66bK1AcMLn7GHgpIYpKDLKs130_assertion
{
miriam-gene:3497
a
ncit:C16612
.
lld:C0036572
a
ncit:C7057
.
dgn-gda:DGNd0b3afaf73cb50d46330733c57da528c
sio:SIO_000628
miriam-gene:3497
,
lld:C0036572
;
a
sio:SIO_001121
.
}
dgn-np:NP461849.RArdOi_tqaVeBAGFnbu9NR66bK1AcMLn7GHgpIYpKDLKs130_provenance
{
dgn-np:NP461849.RArdOi_tqaVeBAGFnbu9NR66bK1AcMLn7GHgpIYpKDLKs130_assertion
dcterms:description
"[In the current study, we specifically analyzed the syndromes of IGE based on their demographic, clinical, and EEG findings to determine if other than the seizure type(s) and age of onset, there are any other distinctive features to distinguish these syndromes of IGEs from one another.]. 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:23149265
;
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:NP461849.RArdOi_tqaVeBAGFnbu9NR66bK1AcMLn7GHgpIYpKDLKs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:35+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
<
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> , <
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
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dgn-void:disgenetrdf
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}