@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP295473.RAkF4Aq0aAaYtEc5mzmJmd82ufbHs5hxPWfmw_Umt3-K4
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP295473.RAkF4Aq0aAaYtEc5mzmJmd82ufbHs5hxPWfmw_Umt3-K4130_head
{
this:
np:hasAssertion
dgn-np:NP295473.RAkF4Aq0aAaYtEc5mzmJmd82ufbHs5hxPWfmw_Umt3-K4130_assertion
;
np:hasProvenance
dgn-np:NP295473.RAkF4Aq0aAaYtEc5mzmJmd82ufbHs5hxPWfmw_Umt3-K4130_provenance
;
np:hasPublicationInfo
dgn-np:NP295473.RAkF4Aq0aAaYtEc5mzmJmd82ufbHs5hxPWfmw_Umt3-K4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP295473.RAkF4Aq0aAaYtEc5mzmJmd82ufbHs5hxPWfmw_Umt3-K4130_assertion
a
np:Assertion
.
dgn-np:NP295473.RAkF4Aq0aAaYtEc5mzmJmd82ufbHs5hxPWfmw_Umt3-K4130_provenance
a
np:Provenance
.
dgn-np:NP295473.RAkF4Aq0aAaYtEc5mzmJmd82ufbHs5hxPWfmw_Umt3-K4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP295473.RAkF4Aq0aAaYtEc5mzmJmd82ufbHs5hxPWfmw_Umt3-K4130_assertion
{
miriam-gene:3786
a
ncit:C16612
.
lld:C0014544
a
ncit:C7057
.
dgn-gda:DGN4dd83563ac54184e1e6b0eb3e1fd8d21
sio:SIO_000628
miriam-gene:3786
,
lld:C0014544
;
a
sio:SIO_001121
.
}
dgn-np:NP295473.RAkF4Aq0aAaYtEc5mzmJmd82ufbHs5hxPWfmw_Umt3-K4130_provenance
{
dgn-np:NP295473.RAkF4Aq0aAaYtEc5mzmJmd82ufbHs5hxPWfmw_Umt3-K4130_assertion
dcterms:description
"[Mutations in two neuronal voltage-gated potassium channel genes (KCNQ2 and KCNQ3) have already been shown to cause epilepsy (BFNC), and we now tested the hypothesis that genetic variation in the KCNQ3 gene confers liability to common IGE subtypes.]. 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:10996506
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP295473.RAkF4Aq0aAaYtEc5mzmJmd82ufbHs5hxPWfmw_Umt3-K4130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:43:59+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}