@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP568415.RA8gZkI7yuHLEJAJlsNEgol3mSlDIuhL6uSLWJ3bJBQOg
> .
@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:NP568415.RA8gZkI7yuHLEJAJlsNEgol3mSlDIuhL6uSLWJ3bJBQOg130_head
{
this:
np:hasAssertion
dgn-np:NP568415.RA8gZkI7yuHLEJAJlsNEgol3mSlDIuhL6uSLWJ3bJBQOg130_assertion
;
np:hasProvenance
dgn-np:NP568415.RA8gZkI7yuHLEJAJlsNEgol3mSlDIuhL6uSLWJ3bJBQOg130_provenance
;
np:hasPublicationInfo
dgn-np:NP568415.RA8gZkI7yuHLEJAJlsNEgol3mSlDIuhL6uSLWJ3bJBQOg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP568415.RA8gZkI7yuHLEJAJlsNEgol3mSlDIuhL6uSLWJ3bJBQOg130_assertion
a
np:Assertion
.
dgn-np:NP568415.RA8gZkI7yuHLEJAJlsNEgol3mSlDIuhL6uSLWJ3bJBQOg130_provenance
a
np:Provenance
.
dgn-np:NP568415.RA8gZkI7yuHLEJAJlsNEgol3mSlDIuhL6uSLWJ3bJBQOg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP568415.RA8gZkI7yuHLEJAJlsNEgol3mSlDIuhL6uSLWJ3bJBQOg130_assertion
{
miriam-gene:3785
a
ncit:C16612
.
lld:C1852581
a
ncit:C7057
.
dgn-gda:DGNbe862f66413c08d8350516513bca344f
sio:SIO_000628
miriam-gene:3785
,
lld:C1852581
;
a
sio:SIO_001121
.
}
dgn-np:NP568415.RA8gZkI7yuHLEJAJlsNEgol3mSlDIuhL6uSLWJ3bJBQOg130_provenance
{
dgn-np:NP568415.RA8gZkI7yuHLEJAJlsNEgol3mSlDIuhL6uSLWJ3bJBQOg130_assertion
dcterms:description
"[This review is focused on recent findings on the neuronal K(V)7 channelopathies, in particular on benign familial neonatal seizures (BFNS) and peripheral nerve hyperexcitability (PNH, neuromyotonia, myokymia) caused by KCNQ2 mutations.]. 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:18238816
;
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 .
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dgn-np:NP568415.RA8gZkI7yuHLEJAJlsNEgol3mSlDIuhL6uSLWJ3bJBQOg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:43+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
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"v2.1.0" .
}