@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP43774.RAgDrCap96LY7aOJoDZ7X3JUadYszCEhQU189mo2PyyZ8
> .
@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 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:NP43774.RAgDrCap96LY7aOJoDZ7X3JUadYszCEhQU189mo2PyyZ8130_head
{
this:
np:hasAssertion
dgn-np:NP43774.RAgDrCap96LY7aOJoDZ7X3JUadYszCEhQU189mo2PyyZ8130_assertion
;
np:hasProvenance
dgn-np:NP43774.RAgDrCap96LY7aOJoDZ7X3JUadYszCEhQU189mo2PyyZ8130_provenance
;
np:hasPublicationInfo
dgn-np:NP43774.RAgDrCap96LY7aOJoDZ7X3JUadYszCEhQU189mo2PyyZ8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP43774.RAgDrCap96LY7aOJoDZ7X3JUadYszCEhQU189mo2PyyZ8130_assertion
a
np:Assertion
.
dgn-np:NP43774.RAgDrCap96LY7aOJoDZ7X3JUadYszCEhQU189mo2PyyZ8130_provenance
a
np:Provenance
.
dgn-np:NP43774.RAgDrCap96LY7aOJoDZ7X3JUadYszCEhQU189mo2PyyZ8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP43774.RAgDrCap96LY7aOJoDZ7X3JUadYszCEhQU189mo2PyyZ8130_assertion
{
miriam-gene:2555
a
ncit:C16612
.
lld:C0004352
a
ncit:C7057
.
dgn-gda:DGN11e33ae0ce4c6c2b4b1926f1071b426a
sio:SIO_000628
miriam-gene:2555
,
lld:C0004352
;
a
sio:SIO_001122
.
}
dgn-np:NP43774.RAgDrCap96LY7aOJoDZ7X3JUadYszCEhQU189mo2PyyZ8130_provenance
{
dgn-np:NP43774.RAgDrCap96LY7aOJoDZ7X3JUadYszCEhQU189mo2PyyZ8130_assertion
dct:description
"[We conclude that GABRA4 is involved in the etiology of autism and potentially increases autism risk through interaction with GABRB1. These results support the hypothesis that GABA receptor subunit genes are involved in autism, most likely via complex gene-gene interactions.]. 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:16080114
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP43774.RAgDrCap96LY7aOJoDZ7X3JUadYszCEhQU189mo2PyyZ8130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:20+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}