@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP479907.RAFadzv6fEz-FYe_SR8ArBUJEPjwyGVqbF5bhs97PA31M
> .
@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:NP479907.RAFadzv6fEz-FYe_SR8ArBUJEPjwyGVqbF5bhs97PA31M130_head
{
this:
np:hasAssertion
dgn-np:NP479907.RAFadzv6fEz-FYe_SR8ArBUJEPjwyGVqbF5bhs97PA31M130_assertion
;
np:hasProvenance
dgn-np:NP479907.RAFadzv6fEz-FYe_SR8ArBUJEPjwyGVqbF5bhs97PA31M130_provenance
;
np:hasPublicationInfo
dgn-np:NP479907.RAFadzv6fEz-FYe_SR8ArBUJEPjwyGVqbF5bhs97PA31M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP479907.RAFadzv6fEz-FYe_SR8ArBUJEPjwyGVqbF5bhs97PA31M130_assertion
a
np:Assertion
.
dgn-np:NP479907.RAFadzv6fEz-FYe_SR8ArBUJEPjwyGVqbF5bhs97PA31M130_provenance
a
np:Provenance
.
dgn-np:NP479907.RAFadzv6fEz-FYe_SR8ArBUJEPjwyGVqbF5bhs97PA31M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP479907.RAFadzv6fEz-FYe_SR8ArBUJEPjwyGVqbF5bhs97PA31M130_assertion
{
miriam-gene:1139
a
ncit:C16612
.
lld:C0085541
a
ncit:C7057
.
dgn-gda:DGNdb2f6e368bacb9739fe47c22d3dd9245
sio:SIO_000628
miriam-gene:1139
,
lld:C0085541
;
a
sio:SIO_001121
.
}
dgn-np:NP479907.RAFadzv6fEz-FYe_SR8ArBUJEPjwyGVqbF5bhs97PA31M130_provenance
{
dgn-np:NP479907.RAFadzv6fEz-FYe_SR8ArBUJEPjwyGVqbF5bhs97PA31M130_assertion
dcterms:description
"[It has been suggested that the homomer-forming α7 subunit (CHRNA7) of the neuronal nicotinic acetylcholine receptor (nAChR) is involved in the pathogenesis of common idiopathic generalized epilepsies (IGEs), whereas mutations of the gene coding for the α4 nAChR subunit (CHRNA4) are associated with autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE).]. 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:23553139
;
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:NP479907.RAFadzv6fEz-FYe_SR8ArBUJEPjwyGVqbF5bhs97PA31M130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:47+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" .
}