@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP927771.RAthXHuB3gVMS-X4laHQn6USupQb1HfhnxvQq7UuC9JlU
> .
@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:NP927771.RAthXHuB3gVMS-X4laHQn6USupQb1HfhnxvQq7UuC9JlU130_head
{
this:
np:hasAssertion
dgn-np:NP927771.RAthXHuB3gVMS-X4laHQn6USupQb1HfhnxvQq7UuC9JlU130_assertion
;
np:hasProvenance
dgn-np:NP927771.RAthXHuB3gVMS-X4laHQn6USupQb1HfhnxvQq7UuC9JlU130_provenance
;
np:hasPublicationInfo
dgn-np:NP927771.RAthXHuB3gVMS-X4laHQn6USupQb1HfhnxvQq7UuC9JlU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP927771.RAthXHuB3gVMS-X4laHQn6USupQb1HfhnxvQq7UuC9JlU130_assertion
a
np:Assertion
.
dgn-np:NP927771.RAthXHuB3gVMS-X4laHQn6USupQb1HfhnxvQq7UuC9JlU130_provenance
a
np:Provenance
.
dgn-np:NP927771.RAthXHuB3gVMS-X4laHQn6USupQb1HfhnxvQq7UuC9JlU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP927771.RAthXHuB3gVMS-X4laHQn6USupQb1HfhnxvQq7UuC9JlU130_assertion
{
miriam-gene:9211
a
ncit:C16612
.
lld:C0014548
a
ncit:C7057
.
dgn-gda:DGN43ac7e134b3be43e0e9d92df6e15b32d
sio:SIO_000628
miriam-gene:9211
,
lld:C0014548
;
a
sio:SIO_001121
.
}
dgn-np:NP927771.RAthXHuB3gVMS-X4laHQn6USupQb1HfhnxvQq7UuC9JlU130_provenance
{
dgn-np:NP927771.RAthXHuB3gVMS-X4laHQn6USupQb1HfhnxvQq7UuC9JlU130_assertion
dcterms:description
"[Mutation of LGI1 gene has been identified in familial lateral temporal lobe epilepsy while mutations of genes which encode sodium channels and GABAA receptors have been reported in generalized epilepsy with febrile seizure plus.]. 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:17981785
;
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:NP927771.RAthXHuB3gVMS-X4laHQn6USupQb1HfhnxvQq7UuC9JlU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:29+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" .
}