@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP560474.RAqClVM53lOV5U1QnWtMbmmsXu7Qwr6GmW6tZsOllbYO8
> .
@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:NP560474.RAqClVM53lOV5U1QnWtMbmmsXu7Qwr6GmW6tZsOllbYO8130_head
{
this:
np:hasAssertion
dgn-np:NP560474.RAqClVM53lOV5U1QnWtMbmmsXu7Qwr6GmW6tZsOllbYO8130_assertion
;
np:hasProvenance
dgn-np:NP560474.RAqClVM53lOV5U1QnWtMbmmsXu7Qwr6GmW6tZsOllbYO8130_provenance
;
np:hasPublicationInfo
dgn-np:NP560474.RAqClVM53lOV5U1QnWtMbmmsXu7Qwr6GmW6tZsOllbYO8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP560474.RAqClVM53lOV5U1QnWtMbmmsXu7Qwr6GmW6tZsOllbYO8130_assertion
a
np:Assertion
.
dgn-np:NP560474.RAqClVM53lOV5U1QnWtMbmmsXu7Qwr6GmW6tZsOllbYO8130_provenance
a
np:Provenance
.
dgn-np:NP560474.RAqClVM53lOV5U1QnWtMbmmsXu7Qwr6GmW6tZsOllbYO8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP560474.RAqClVM53lOV5U1QnWtMbmmsXu7Qwr6GmW6tZsOllbYO8130_assertion
{
miriam-gene:759
a
ncit:C16612
.
lld:C0014544
a
ncit:C7057
.
dgn-gda:DGN1efcef812cfb8d281a042d07a50174fc
sio:SIO_000628
miriam-gene:759
,
lld:C0014544
;
a
sio:SIO_001121
.
}
dgn-np:NP560474.RAqClVM53lOV5U1QnWtMbmmsXu7Qwr6GmW6tZsOllbYO8130_provenance
{
dgn-np:NP560474.RAqClVM53lOV5U1QnWtMbmmsXu7Qwr6GmW6tZsOllbYO8130_assertion
dcterms:description
"[Computational modelling experiments in CA1 pyramidal cells revealed that the gating changes introduced by the K(v)7.2 D212G increased cell firing frequency, thereby triggering the neuronal hyperexcitability which underlies the observed neonatal epileptic condition.]. 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:19344764
;
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:NP560474.RAqClVM53lOV5U1QnWtMbmmsXu7Qwr6GmW6tZsOllbYO8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:38+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" .
}