@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP895746.RAHXPsQdC2lbUwwBikZ72OgmY3Nzx83rRmCQC6ulKRVzc
> .
@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:NP895746.RAHXPsQdC2lbUwwBikZ72OgmY3Nzx83rRmCQC6ulKRVzc130_head
{
this:
np:hasAssertion
dgn-np:NP895746.RAHXPsQdC2lbUwwBikZ72OgmY3Nzx83rRmCQC6ulKRVzc130_assertion
;
np:hasProvenance
dgn-np:NP895746.RAHXPsQdC2lbUwwBikZ72OgmY3Nzx83rRmCQC6ulKRVzc130_provenance
;
np:hasPublicationInfo
dgn-np:NP895746.RAHXPsQdC2lbUwwBikZ72OgmY3Nzx83rRmCQC6ulKRVzc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP895746.RAHXPsQdC2lbUwwBikZ72OgmY3Nzx83rRmCQC6ulKRVzc130_assertion
a
np:Assertion
.
dgn-np:NP895746.RAHXPsQdC2lbUwwBikZ72OgmY3Nzx83rRmCQC6ulKRVzc130_provenance
a
np:Provenance
.
dgn-np:NP895746.RAHXPsQdC2lbUwwBikZ72OgmY3Nzx83rRmCQC6ulKRVzc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP895746.RAHXPsQdC2lbUwwBikZ72OgmY3Nzx83rRmCQC6ulKRVzc130_assertion
{
miriam-gene:3785
a
ncit:C16612
.
lld:C0085541
a
ncit:C7057
.
dgn-gda:DGN80abcebdac996e1b15a29e12fa5edbc6
sio:SIO_000628
miriam-gene:3785
,
lld:C0085541
;
a
sio:SIO_001121
.
}
dgn-np:NP895746.RAHXPsQdC2lbUwwBikZ72OgmY3Nzx83rRmCQC6ulKRVzc130_provenance
{
dgn-np:NP895746.RAHXPsQdC2lbUwwBikZ72OgmY3Nzx83rRmCQC6ulKRVzc130_assertion
dcterms:description
"[The clinical courses of patients with deletions of both KCNQ2 and CHRNA4 were those of typical BFNS, and none presented with the phenotype of autosomal dominant nocturnal frontal lobe epilepsy, some of which are caused by mutations of CHRNA4.]. 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:19822871
;
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:NP895746.RAHXPsQdC2lbUwwBikZ72OgmY3Nzx83rRmCQC6ulKRVzc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:10+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" .
}