@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP416711.RAvKoBEf2axBXPT8u6njNxsw7oTGbB5ReJvKdxsjsQ7Bw
> .
@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/v3.0.0/void/
> .
dgn-np:NP416711.RAvKoBEf2axBXPT8u6njNxsw7oTGbB5ReJvKdxsjsQ7Bw130_head
{
this:
np:hasAssertion
dgn-np:NP416711.RAvKoBEf2axBXPT8u6njNxsw7oTGbB5ReJvKdxsjsQ7Bw130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
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a
np:Nanopublication
.
dgn-np:NP416711.RAvKoBEf2axBXPT8u6njNxsw7oTGbB5ReJvKdxsjsQ7Bw130_assertion
a
np:Assertion
.
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a
np:Provenance
.
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a
np:PublicationInfo
.
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{
miriam-gene:2554
a
ncit:C16612
.
lld:C0014544
a
ncit:C7057
.
dgn-gda:DGN29e61a4eccfe06aab4e6a0e508b6c4f5
sio:SIO_000628
miriam-gene:2554
,
lld:C0014544
;
a
sio:SIO_001122
.
}
dgn-np:NP416711.RAvKoBEf2axBXPT8u6njNxsw7oTGbB5ReJvKdxsjsQ7Bw130_provenance
{
dgn-np:NP416711.RAvKoBEf2axBXPT8u6njNxsw7oTGbB5ReJvKdxsjsQ7Bw130_assertion
dcterms:description
"[Further multivariate logistic regression and multifactor dimensionality reduction analyses of interactions between these genes showed that under adjustment of clinical factors, the epilepsy treatment outcomes were significantly associated with the genotype combinations of GABRA1 rs6883877, GABRA2 rs511310 and GABRA3 rs4828696 (p < 0.0001; adjusted r(2) = 0.149).]. 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:24236484
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP416711.RAvKoBEf2axBXPT8u6njNxsw7oTGbB5ReJvKdxsjsQ7Bw130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:41:42+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
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;
pav:authoredBy
<
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> , <
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
"v3.0.0.0" .
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pav:version
"v3.0.0" .
}