@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP490311.RADSgP-AUvyPCo931xLIel7o00QJt-e3xKBSbhoTMe2hs
> .
@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/v4.0.0/void/
> .
dgn-np:NP490311.RADSgP-AUvyPCo931xLIel7o00QJt-e3xKBSbhoTMe2hs130_head
{
this:
np:hasAssertion
dgn-np:NP490311.RADSgP-AUvyPCo931xLIel7o00QJt-e3xKBSbhoTMe2hs130_assertion
;
np:hasProvenance
dgn-np:NP490311.RADSgP-AUvyPCo931xLIel7o00QJt-e3xKBSbhoTMe2hs130_provenance
;
np:hasPublicationInfo
dgn-np:NP490311.RADSgP-AUvyPCo931xLIel7o00QJt-e3xKBSbhoTMe2hs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP490311.RADSgP-AUvyPCo931xLIel7o00QJt-e3xKBSbhoTMe2hs130_assertion
a
np:Assertion
.
dgn-np:NP490311.RADSgP-AUvyPCo931xLIel7o00QJt-e3xKBSbhoTMe2hs130_provenance
a
np:Provenance
.
dgn-np:NP490311.RADSgP-AUvyPCo931xLIel7o00QJt-e3xKBSbhoTMe2hs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP490311.RADSgP-AUvyPCo931xLIel7o00QJt-e3xKBSbhoTMe2hs130_assertion
{
miriam-gene:2555
a
ncit:C16612
.
lld:C0001973
a
ncit:C7057
.
dgn-gda:DGN2de7e0edd31707fa72bc2e65c1422d7a
sio:SIO_000628
miriam-gene:2555
,
lld:C0001973
;
a
sio:SIO_001121
.
}
dgn-np:NP490311.RADSgP-AUvyPCo931xLIel7o00QJt-e3xKBSbhoTMe2hs130_provenance
{
dgn-np:NP490311.RADSgP-AUvyPCo931xLIel7o00QJt-e3xKBSbhoTMe2hs130_assertion
dcterms:description
"[These findings suggest that genetic variants of GABRA2 increase risk for AD in the Russian population and provide additional support to the hypothesis that polymorphic variation at the GABRA2 locus plays an important role in predisposing to AD at least in European-ancestry populations.]. 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:15834213
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP490311.RADSgP-AUvyPCo931xLIel7o00QJt-e3xKBSbhoTMe2hs130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:27+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
<
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
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