@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP43769.RASw339x4DsLSLHTRDih4srvBPGsik1TvR_PtZtptZQ4w
> .
@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:NP43769.RASw339x4DsLSLHTRDih4srvBPGsik1TvR_PtZtptZQ4w130_head
{
this:
np:hasAssertion
dgn-np:NP43769.RASw339x4DsLSLHTRDih4srvBPGsik1TvR_PtZtptZQ4w130_assertion
;
np:hasProvenance
dgn-np:NP43769.RASw339x4DsLSLHTRDih4srvBPGsik1TvR_PtZtptZQ4w130_provenance
;
np:hasPublicationInfo
dgn-np:NP43769.RASw339x4DsLSLHTRDih4srvBPGsik1TvR_PtZtptZQ4w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP43769.RASw339x4DsLSLHTRDih4srvBPGsik1TvR_PtZtptZQ4w130_assertion
a
np:Assertion
.
dgn-np:NP43769.RASw339x4DsLSLHTRDih4srvBPGsik1TvR_PtZtptZQ4w130_provenance
a
np:Provenance
.
dgn-np:NP43769.RASw339x4DsLSLHTRDih4srvBPGsik1TvR_PtZtptZQ4w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP43769.RASw339x4DsLSLHTRDih4srvBPGsik1TvR_PtZtptZQ4w130_assertion
{
miriam-gene:2557
a
ncit:C16612
.
lld:C0004352
a
ncit:C7057
.
dgn-gda:DGN12494ae1233fb5084f0e5cd2739ce09f
sio:SIO_000628
miriam-gene:2557
,
lld:C0004352
;
a
sio:SIO_001122
.
}
dgn-np:NP43769.RASw339x4DsLSLHTRDih4srvBPGsik1TvR_PtZtptZQ4w130_provenance
{
dgn-np:NP43769.RASw339x4DsLSLHTRDih4srvBPGsik1TvR_PtZtptZQ4w130_assertion
dcterms: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:NP43769.RASw339x4DsLSLHTRDih4srvBPGsik1TvR_PtZtptZQ4w130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:20+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" .
}