@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP918158.RA11WnO5zSS8aqcBpfnstV98hnCw28g11DoBpC1C4pJws
> .
@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:NP918158.RA11WnO5zSS8aqcBpfnstV98hnCw28g11DoBpC1C4pJws130_head
{
this:
np:hasAssertion
dgn-np:NP918158.RA11WnO5zSS8aqcBpfnstV98hnCw28g11DoBpC1C4pJws130_assertion
;
np:hasProvenance
dgn-np:NP918158.RA11WnO5zSS8aqcBpfnstV98hnCw28g11DoBpC1C4pJws130_provenance
;
np:hasPublicationInfo
dgn-np:NP918158.RA11WnO5zSS8aqcBpfnstV98hnCw28g11DoBpC1C4pJws130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP918158.RA11WnO5zSS8aqcBpfnstV98hnCw28g11DoBpC1C4pJws130_assertion
a
np:Assertion
.
dgn-np:NP918158.RA11WnO5zSS8aqcBpfnstV98hnCw28g11DoBpC1C4pJws130_provenance
a
np:Provenance
.
dgn-np:NP918158.RA11WnO5zSS8aqcBpfnstV98hnCw28g11DoBpC1C4pJws130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP918158.RA11WnO5zSS8aqcBpfnstV98hnCw28g11DoBpC1C4pJws130_assertion
{
miriam-gene:2566
a
ncit:C16612
.
lld:C3502809
a
ncit:C7057
.
dgn-gda:DGN8c22231dfe728668e3954e0b4fe9314d
sio:SIO_000628
miriam-gene:2566
,
lld:C3502809
;
a
sio:SIO_001121
.
}
dgn-np:NP918158.RA11WnO5zSS8aqcBpfnstV98hnCw28g11DoBpC1C4pJws130_provenance
{
dgn-np:NP918158.RA11WnO5zSS8aqcBpfnstV98hnCw28g11DoBpC1C4pJws130_assertion
dcterms:description
"[The voltage-gated sodium channel subunits SCN1B, SCN1A and SCN2A as well as the GABRG2 subunit of the GABA(A) receptor are involved in the pathology of the newly described syndrome generalized epilepsy with febrile seizures 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:11888238
;
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:NP918158.RA11WnO5zSS8aqcBpfnstV98hnCw28g11DoBpC1C4pJws130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:23+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" .
}