@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP925477.RAHKaryJ-9x_WqN9bqf5-F7oHPcWzP88pYBUtLH9DQOuQ
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP925477.RAHKaryJ-9x_WqN9bqf5-F7oHPcWzP88pYBUtLH9DQOuQ130_assertion
;
np:hasProvenance
dgn-np:NP925477.RAHKaryJ-9x_WqN9bqf5-F7oHPcWzP88pYBUtLH9DQOuQ130_provenance
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np:hasPublicationInfo
dgn-np:NP925477.RAHKaryJ-9x_WqN9bqf5-F7oHPcWzP88pYBUtLH9DQOuQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP925477.RAHKaryJ-9x_WqN9bqf5-F7oHPcWzP88pYBUtLH9DQOuQ130_assertion
a
np:Assertion
.
dgn-np:NP925477.RAHKaryJ-9x_WqN9bqf5-F7oHPcWzP88pYBUtLH9DQOuQ130_provenance
a
np:Provenance
.
dgn-np:NP925477.RAHKaryJ-9x_WqN9bqf5-F7oHPcWzP88pYBUtLH9DQOuQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP925477.RAHKaryJ-9x_WqN9bqf5-F7oHPcWzP88pYBUtLH9DQOuQ130_assertion
{
miriam-gene:3785
a
ncit:C16612
.
lld:C0085584
a
ncit:C7057
.
dgn-gda:DGN767f9161c86b068ba68007df795fde15
sio:SIO_000628
miriam-gene:3785
,
lld:C0085584
;
a
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.
}
dgn-np:NP925477.RAHKaryJ-9x_WqN9bqf5-F7oHPcWzP88pYBUtLH9DQOuQ130_provenance
{
dgn-np:NP925477.RAHKaryJ-9x_WqN9bqf5-F7oHPcWzP88pYBUtLH9DQOuQ130_assertion
dcterms:description
"[Our objective was to confirm that KCNQ2 was an important gene to include in the diagnosis workup of EOEEs and to fully describe the clinical and EEG features of mutated patients.]. 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:23692823
;
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:NP925477.RAHKaryJ-9x_WqN9bqf5-F7oHPcWzP88pYBUtLH9DQOuQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:27+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" .
}