@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP923779.RAtCht87qnqp93tqr0DdAJy-gXYuiavh6d3ewUjI2mR7I
> .
@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:NP923779.RAtCht87qnqp93tqr0DdAJy-gXYuiavh6d3ewUjI2mR7I130_head
{
this:
np:hasAssertion
dgn-np:NP923779.RAtCht87qnqp93tqr0DdAJy-gXYuiavh6d3ewUjI2mR7I130_assertion
;
np:hasProvenance
dgn-np:NP923779.RAtCht87qnqp93tqr0DdAJy-gXYuiavh6d3ewUjI2mR7I130_provenance
;
np:hasPublicationInfo
dgn-np:NP923779.RAtCht87qnqp93tqr0DdAJy-gXYuiavh6d3ewUjI2mR7I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP923779.RAtCht87qnqp93tqr0DdAJy-gXYuiavh6d3ewUjI2mR7I130_assertion
a
np:Assertion
.
dgn-np:NP923779.RAtCht87qnqp93tqr0DdAJy-gXYuiavh6d3ewUjI2mR7I130_provenance
a
np:Provenance
.
dgn-np:NP923779.RAtCht87qnqp93tqr0DdAJy-gXYuiavh6d3ewUjI2mR7I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP923779.RAtCht87qnqp93tqr0DdAJy-gXYuiavh6d3ewUjI2mR7I130_assertion
{
miriam-gene:3497
a
ncit:C16612
.
lld:C0014548
a
ncit:C7057
.
dgn-gda:DGN9576d800e86770702736eded5f3b562a
sio:SIO_000628
miriam-gene:3497
,
lld:C0014548
;
a
sio:SIO_001121
.
}
dgn-np:NP923779.RAtCht87qnqp93tqr0DdAJy-gXYuiavh6d3ewUjI2mR7I130_provenance
{
dgn-np:NP923779.RAtCht87qnqp93tqr0DdAJy-gXYuiavh6d3ewUjI2mR7I130_assertion
dcterms:description
"[This study aims to examine the clinical and EEG features of probands with JME and to identify the incidence of different types of idiopathic generalized epilepsies (IGEs) and IGE trait in first-degree relatives.]. 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:16495091
;
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:NP923779.RAtCht87qnqp93tqr0DdAJy-gXYuiavh6d3ewUjI2mR7I130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:26+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" .
}