@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP311731.RA-oiu4XLeftXlFCBDtXgc-DSt1_ZVABi0j35P0eu3nh0
> .
@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:NP311731.RA-oiu4XLeftXlFCBDtXgc-DSt1_ZVABi0j35P0eu3nh0130_head
{
this:
np:hasAssertion
dgn-np:NP311731.RA-oiu4XLeftXlFCBDtXgc-DSt1_ZVABi0j35P0eu3nh0130_assertion
;
np:hasProvenance
dgn-np:NP311731.RA-oiu4XLeftXlFCBDtXgc-DSt1_ZVABi0j35P0eu3nh0130_provenance
;
np:hasPublicationInfo
dgn-np:NP311731.RA-oiu4XLeftXlFCBDtXgc-DSt1_ZVABi0j35P0eu3nh0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP311731.RA-oiu4XLeftXlFCBDtXgc-DSt1_ZVABi0j35P0eu3nh0130_assertion
a
np:Assertion
.
dgn-np:NP311731.RA-oiu4XLeftXlFCBDtXgc-DSt1_ZVABi0j35P0eu3nh0130_provenance
a
np:Provenance
.
dgn-np:NP311731.RA-oiu4XLeftXlFCBDtXgc-DSt1_ZVABi0j35P0eu3nh0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP311731.RA-oiu4XLeftXlFCBDtXgc-DSt1_ZVABi0j35P0eu3nh0130_assertion
{
miriam-gene:100379198
a
ncit:C16612
.
lld:C0220669
a
ncit:C7057
.
dgn-gda:DGN0d32ab6345cf45befb53cecb5525a9c4
sio:SIO_000628
miriam-gene:100379198
,
lld:C0220669
;
a
sio:SIO_001121
.
}
dgn-np:NP311731.RA-oiu4XLeftXlFCBDtXgc-DSt1_ZVABi0j35P0eu3nh0130_provenance
{
dgn-np:NP311731.RA-oiu4XLeftXlFCBDtXgc-DSt1_ZVABi0j35P0eu3nh0130_assertion
dcterms:description
"[The molecular pathogenesis of benign childhood epilepsy with centrotemporal spikes (BECTS) remains unclear whereas mutations of the KCNQ2 and KCNQ3 genes have been identified as causes of benign familial neonatal convulsions.]. 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:22884718
;
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:NP311731.RA-oiu4XLeftXlFCBDtXgc-DSt1_ZVABi0j35P0eu3nh0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:59+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" .
}