@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP327522.RAKvYfnDc50jNLEDr2gICIwiJQBoDplnkVAIYzCn4KLp0
> .
@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:NP327522.RAKvYfnDc50jNLEDr2gICIwiJQBoDplnkVAIYzCn4KLp0130_head
{
this:
np:hasAssertion
dgn-np:NP327522.RAKvYfnDc50jNLEDr2gICIwiJQBoDplnkVAIYzCn4KLp0130_assertion
;
np:hasProvenance
dgn-np:NP327522.RAKvYfnDc50jNLEDr2gICIwiJQBoDplnkVAIYzCn4KLp0130_provenance
;
np:hasPublicationInfo
dgn-np:NP327522.RAKvYfnDc50jNLEDr2gICIwiJQBoDplnkVAIYzCn4KLp0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP327522.RAKvYfnDc50jNLEDr2gICIwiJQBoDplnkVAIYzCn4KLp0130_assertion
a
np:Assertion
.
dgn-np:NP327522.RAKvYfnDc50jNLEDr2gICIwiJQBoDplnkVAIYzCn4KLp0130_provenance
a
np:Provenance
.
dgn-np:NP327522.RAKvYfnDc50jNLEDr2gICIwiJQBoDplnkVAIYzCn4KLp0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP327522.RAKvYfnDc50jNLEDr2gICIwiJQBoDplnkVAIYzCn4KLp0130_assertion
{
miriam-gene:2566
a
ncit:C16612
.
lld:C0752203
a
ncit:C7057
.
dgn-gda:DGNb070c5e54a776aa915c6d6adda4b0001
sio:SIO_000628
miriam-gene:2566
,
lld:C0752203
;
a
sio:SIO_001121
.
}
dgn-np:NP327522.RAKvYfnDc50jNLEDr2gICIwiJQBoDplnkVAIYzCn4KLp0130_provenance
{
dgn-np:NP327522.RAKvYfnDc50jNLEDr2gICIwiJQBoDplnkVAIYzCn4KLp0130_assertion
dcterms:description
"[In this study, we tested the hypothesis that mutations in the GABRA1, GABRB3, and GABRG2 genes encoding the alpha1, beta3, and gamma subunits of the GABA(A) receptor are involved in familial primary dystonia.]. 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:17880575
;
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:NP327522.RAKvYfnDc50jNLEDr2gICIwiJQBoDplnkVAIYzCn4KLp0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:11+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" .
}