@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP707874.RAcG-g5TuA8Sz2HhhO399Y_q3tAars5UHAU7UhEjFUeVg
> .
@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:NP707874.RAcG-g5TuA8Sz2HhhO399Y_q3tAars5UHAU7UhEjFUeVg130_head
{
this:
np:hasAssertion
dgn-np:NP707874.RAcG-g5TuA8Sz2HhhO399Y_q3tAars5UHAU7UhEjFUeVg130_assertion
;
np:hasProvenance
dgn-np:NP707874.RAcG-g5TuA8Sz2HhhO399Y_q3tAars5UHAU7UhEjFUeVg130_provenance
;
np:hasPublicationInfo
dgn-np:NP707874.RAcG-g5TuA8Sz2HhhO399Y_q3tAars5UHAU7UhEjFUeVg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP707874.RAcG-g5TuA8Sz2HhhO399Y_q3tAars5UHAU7UhEjFUeVg130_assertion
a
np:Assertion
.
dgn-np:NP707874.RAcG-g5TuA8Sz2HhhO399Y_q3tAars5UHAU7UhEjFUeVg130_provenance
a
np:Provenance
.
dgn-np:NP707874.RAcG-g5TuA8Sz2HhhO399Y_q3tAars5UHAU7UhEjFUeVg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP707874.RAcG-g5TuA8Sz2HhhO399Y_q3tAars5UHAU7UhEjFUeVg130_assertion
{
miriam-gene:9211
a
ncit:C16612
.
lld:C1838062
a
ncit:C7057
.
dgn-gda:DGNee878eee33d37cf4d469b561eb863733
sio:SIO_000628
miriam-gene:9211
,
lld:C1838062
;
a
sio:SIO_001121
.
}
dgn-np:NP707874.RAcG-g5TuA8Sz2HhhO399Y_q3tAars5UHAU7UhEjFUeVg130_provenance
{
dgn-np:NP707874.RAcG-g5TuA8Sz2HhhO399Y_q3tAars5UHAU7UhEjFUeVg130_assertion
dcterms:description
"[Autosomal dominant partial epilepsy with auditory features (ADPEAF) is an idiopathic focal epilepsy syndrome with auditory symptoms or receptive aphasia as major ictal manifestations, frequently associated with mutations in the leucine-rich, glioma inactivated 1 (LGI1) gene.]. 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:19064878
;
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:NP707874.RAcG-g5TuA8Sz2HhhO399Y_q3tAars5UHAU7UhEjFUeVg130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:06+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:disgenetv3.0rdf
;
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" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}