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http://rdf.disgenet.org/nanopublications.trig#NP206813.RAl7EBKEJfXHpdvfy53LRVluhHcW544xgeiBun94lGPXQ
> .
@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#
> .
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{
this:
np:hasAssertion
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np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP206813.RAl7EBKEJfXHpdvfy53LRVluhHcW544xgeiBun94lGPXQ130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP206813.RAl7EBKEJfXHpdvfy53LRVluhHcW544xgeiBun94lGPXQ130_assertion
a
np:Assertion
.
dgn-np:NP206813.RAl7EBKEJfXHpdvfy53LRVluhHcW544xgeiBun94lGPXQ130_provenance
a
np:Provenance
.
dgn-np:NP206813.RAl7EBKEJfXHpdvfy53LRVluhHcW544xgeiBun94lGPXQ130_publicationInfo
a
np:PublicationInfo
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dgn-np:NP206813.RAl7EBKEJfXHpdvfy53LRVluhHcW544xgeiBun94lGPXQ130_assertion
{
miriam-gene:1137
a
ncit:C16612
.
lld:C0270853
a
ncit:C7057
.
dgn-gda:DGN3c41b3bacbb5b8ee3b527ed0828649cb
sio:SIO_000628
miriam-gene:1137
,
lld:C0270853
;
a
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.
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dgn-np:NP206813.RAl7EBKEJfXHpdvfy53LRVluhHcW544xgeiBun94lGPXQ130_provenance
{
dgn-np:NP206813.RAl7EBKEJfXHpdvfy53LRVluhHcW544xgeiBun94lGPXQ130_assertion
dcterms:description
"[In the present study, we examined the possible role of CHRNA4 in common subtypes of idiopathic generalized epilepsy (IGE), comprising childhood and juvenile absence epilepsy and juvenile myoclonic epilepsy (JME), by systematically screening the coding region of the gene for sequence variants.]. 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:9259383
;
prov:wasDerivedFrom
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;
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:NP206813.RAl7EBKEJfXHpdvfy53LRVluhHcW544xgeiBun94lGPXQ130_publicationInfo
{
this:
dcterms:created
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xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
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pav:authoredBy
<
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> , <
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> , <
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> , <
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http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
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