@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP783585.RAloRAFdH5EXaiZpC5nozMLWRZskuifPItgtGfuLx3xpg
> .
@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:NP783585.RAloRAFdH5EXaiZpC5nozMLWRZskuifPItgtGfuLx3xpg130_head
{
this:
np:hasAssertion
dgn-np:NP783585.RAloRAFdH5EXaiZpC5nozMLWRZskuifPItgtGfuLx3xpg130_assertion
;
np:hasProvenance
dgn-np:NP783585.RAloRAFdH5EXaiZpC5nozMLWRZskuifPItgtGfuLx3xpg130_provenance
;
np:hasPublicationInfo
dgn-np:NP783585.RAloRAFdH5EXaiZpC5nozMLWRZskuifPItgtGfuLx3xpg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP783585.RAloRAFdH5EXaiZpC5nozMLWRZskuifPItgtGfuLx3xpg130_assertion
a
np:Assertion
.
dgn-np:NP783585.RAloRAFdH5EXaiZpC5nozMLWRZskuifPItgtGfuLx3xpg130_provenance
a
np:Provenance
.
dgn-np:NP783585.RAloRAFdH5EXaiZpC5nozMLWRZskuifPItgtGfuLx3xpg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP783585.RAloRAFdH5EXaiZpC5nozMLWRZskuifPItgtGfuLx3xpg130_assertion
{
miriam-gene:1137
a
ncit:C16612
.
lld:C0391957
a
ncit:C7057
.
dgn-gda:DGNc035b8b7b9b5bd500f3ca1352df3da3a
sio:SIO_000628
miriam-gene:1137
,
lld:C0391957
;
a
sio:SIO_001121
.
}
dgn-np:NP783585.RAloRAFdH5EXaiZpC5nozMLWRZskuifPItgtGfuLx3xpg130_provenance
{
dgn-np:NP783585.RAloRAFdH5EXaiZpC5nozMLWRZskuifPItgtGfuLx3xpg130_assertion
dcterms:description
"[The alpha4-subunit gene (CHRNA4) of the neuronal nicotinic acetylcholine receptor (nAChR) subunit family has recently been identified in two families as the gene responsible for autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE), a rare monogenic idiopathic epilepsy.]. 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:9921897
;
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:NP783585.RAloRAFdH5EXaiZpC5nozMLWRZskuifPItgtGfuLx3xpg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:54+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" .
}