@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP862353.RAiW9W92NjF4oeh0SxMJppzBZmR0U_scEEcf3X4wlD_C8
> .
@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:NP862353.RAiW9W92NjF4oeh0SxMJppzBZmR0U_scEEcf3X4wlD_C8130_head
{
this:
np:hasAssertion
dgn-np:NP862353.RAiW9W92NjF4oeh0SxMJppzBZmR0U_scEEcf3X4wlD_C8130_assertion
;
np:hasProvenance
dgn-np:NP862353.RAiW9W92NjF4oeh0SxMJppzBZmR0U_scEEcf3X4wlD_C8130_provenance
;
np:hasPublicationInfo
dgn-np:NP862353.RAiW9W92NjF4oeh0SxMJppzBZmR0U_scEEcf3X4wlD_C8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP862353.RAiW9W92NjF4oeh0SxMJppzBZmR0U_scEEcf3X4wlD_C8130_assertion
a
np:Assertion
.
dgn-np:NP862353.RAiW9W92NjF4oeh0SxMJppzBZmR0U_scEEcf3X4wlD_C8130_provenance
a
np:Provenance
.
dgn-np:NP862353.RAiW9W92NjF4oeh0SxMJppzBZmR0U_scEEcf3X4wlD_C8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP862353.RAiW9W92NjF4oeh0SxMJppzBZmR0U_scEEcf3X4wlD_C8130_assertion
{
miriam-gene:3786
a
ncit:C16612
.
lld:C0270851
a
ncit:C7057
.
dgn-gda:DGNd834dc82695a768b84b97e622cb29cb9
sio:SIO_000628
miriam-gene:3786
,
lld:C0270851
;
a
sio:SIO_001121
.
}
dgn-np:NP862353.RAiW9W92NjF4oeh0SxMJppzBZmR0U_scEEcf3X4wlD_C8130_provenance
{
dgn-np:NP862353.RAiW9W92NjF4oeh0SxMJppzBZmR0U_scEEcf3X4wlD_C8130_assertion
dcterms:description
"[The importance of ionic channels as cause of epilepsies was further demonstrated with the identification of the association between the benign neonatal epilepsy and mutations in genes coding for potassium channel subunits (KCNQ2, KCNQ3).]. 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:11690625
;
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:NP862353.RAiW9W92NjF4oeh0SxMJppzBZmR0U_scEEcf3X4wlD_C8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:47+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" .
}