@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP652235.RAysjvhEAW4m77EDSmexMp5j0KulUFQrFv3PTOiBUZXk4
> .
@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:NP652235.RAysjvhEAW4m77EDSmexMp5j0KulUFQrFv3PTOiBUZXk4130_head
{
this:
np:hasAssertion
dgn-np:NP652235.RAysjvhEAW4m77EDSmexMp5j0KulUFQrFv3PTOiBUZXk4130_assertion
;
np:hasProvenance
dgn-np:NP652235.RAysjvhEAW4m77EDSmexMp5j0KulUFQrFv3PTOiBUZXk4130_provenance
;
np:hasPublicationInfo
dgn-np:NP652235.RAysjvhEAW4m77EDSmexMp5j0KulUFQrFv3PTOiBUZXk4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP652235.RAysjvhEAW4m77EDSmexMp5j0KulUFQrFv3PTOiBUZXk4130_assertion
a
np:Assertion
.
dgn-np:NP652235.RAysjvhEAW4m77EDSmexMp5j0KulUFQrFv3PTOiBUZXk4130_provenance
a
np:Provenance
.
dgn-np:NP652235.RAysjvhEAW4m77EDSmexMp5j0KulUFQrFv3PTOiBUZXk4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP652235.RAysjvhEAW4m77EDSmexMp5j0KulUFQrFv3PTOiBUZXk4130_assertion
{
miriam-gene:1135
a
ncit:C16612
.
lld:C0085541
a
ncit:C7057
.
dgn-gda:DGN69c361d1b499ae0162a61955155895db
sio:SIO_000628
miriam-gene:1135
,
lld:C0085541
;
a
sio:SIO_001121
.
}
dgn-np:NP652235.RAysjvhEAW4m77EDSmexMp5j0KulUFQrFv3PTOiBUZXk4130_provenance
{
dgn-np:NP652235.RAysjvhEAW4m77EDSmexMp5j0KulUFQrFv3PTOiBUZXk4130_assertion
dcterms:description
"[Forty-six nocturnal frontal lobe epilepsy (NFLE) patients (in which the involvement of the CHRNA4 and CHRNB2 genes coding for neuronal nicotinic acetylcholine receptor (nAChRs) subunits associated to the disease were previously excluded) were analyzed for the presence of mutations in the CHRNA2 gene coding for the alpha2 subunit of the same receptor, which has been recently associated with the disease.]. 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:18226955
;
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:NP652235.RAysjvhEAW4m77EDSmexMp5j0KulUFQrFv3PTOiBUZXk4130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:41+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" .
}