@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP761632.RAo4JIHBConBqyoOHa-b2ovdxowmqa9zCYJALZRfkk-vQ
> .
@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:NP761632.RAo4JIHBConBqyoOHa-b2ovdxowmqa9zCYJALZRfkk-vQ130_head
{
this:
np:hasAssertion
dgn-np:NP761632.RAo4JIHBConBqyoOHa-b2ovdxowmqa9zCYJALZRfkk-vQ130_assertion
;
np:hasProvenance
dgn-np:NP761632.RAo4JIHBConBqyoOHa-b2ovdxowmqa9zCYJALZRfkk-vQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP761632.RAo4JIHBConBqyoOHa-b2ovdxowmqa9zCYJALZRfkk-vQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP761632.RAo4JIHBConBqyoOHa-b2ovdxowmqa9zCYJALZRfkk-vQ130_assertion
a
np:Assertion
.
dgn-np:NP761632.RAo4JIHBConBqyoOHa-b2ovdxowmqa9zCYJALZRfkk-vQ130_provenance
a
np:Provenance
.
dgn-np:NP761632.RAo4JIHBConBqyoOHa-b2ovdxowmqa9zCYJALZRfkk-vQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP761632.RAo4JIHBConBqyoOHa-b2ovdxowmqa9zCYJALZRfkk-vQ130_assertion
{
miriam-gene:2566
a
ncit:C16612
.
lld:C0014548
a
ncit:C7057
.
dgn-gda:DGN5aef602a77d47b5dab6d75aa59b88e9b
sio:SIO_000628
miriam-gene:2566
,
lld:C0014548
;
a
sio:SIO_001121
.
}
dgn-np:NP761632.RAo4JIHBConBqyoOHa-b2ovdxowmqa9zCYJALZRfkk-vQ130_provenance
{
dgn-np:NP761632.RAo4JIHBConBqyoOHa-b2ovdxowmqa9zCYJALZRfkk-vQ130_assertion
dcterms:description
"[Our linkage analyses in 63 families ascertained through IGE patients with either juvenile myoclonic epilepsy, juvenile absence epilepsy or childhood absence epilepsy do not support the hypothesis that variants within the GABRA1 and GABRG2 gene cluster contribute a frequent major gene effect to the expression of the common familial IGEs.]. 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:8739126
;
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:NP761632.RAo4JIHBConBqyoOHa-b2ovdxowmqa9zCYJALZRfkk-vQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:41+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" .
}