@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP748252.RAzLE8no3PSWQnM4nNpCXLZEGwAOpvr1eZxSES2Fi8WZY
> .
@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:NP748252.RAzLE8no3PSWQnM4nNpCXLZEGwAOpvr1eZxSES2Fi8WZY130_head
{
this:
np:hasAssertion
dgn-np:NP748252.RAzLE8no3PSWQnM4nNpCXLZEGwAOpvr1eZxSES2Fi8WZY130_assertion
;
np:hasProvenance
dgn-np:NP748252.RAzLE8no3PSWQnM4nNpCXLZEGwAOpvr1eZxSES2Fi8WZY130_provenance
;
np:hasPublicationInfo
dgn-np:NP748252.RAzLE8no3PSWQnM4nNpCXLZEGwAOpvr1eZxSES2Fi8WZY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP748252.RAzLE8no3PSWQnM4nNpCXLZEGwAOpvr1eZxSES2Fi8WZY130_assertion
a
np:Assertion
.
dgn-np:NP748252.RAzLE8no3PSWQnM4nNpCXLZEGwAOpvr1eZxSES2Fi8WZY130_provenance
a
np:Provenance
.
dgn-np:NP748252.RAzLE8no3PSWQnM4nNpCXLZEGwAOpvr1eZxSES2Fi8WZY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP748252.RAzLE8no3PSWQnM4nNpCXLZEGwAOpvr1eZxSES2Fi8WZY130_assertion
{
miriam-gene:414
a
ncit:C16612
.
lld:C0012236
a
ncit:C7057
.
dgn-gda:DGN145787213aaaf9c999bc3a1b30f9a1b9
sio:SIO_000628
miriam-gene:414
,
lld:C0012236
;
a
sio:SIO_001121
.
}
dgn-np:NP748252.RAzLE8no3PSWQnM4nNpCXLZEGwAOpvr1eZxSES2Fi8WZY130_provenance
{
dgn-np:NP748252.RAzLE8no3PSWQnM4nNpCXLZEGwAOpvr1eZxSES2Fi8WZY130_assertion
dcterms:description
"[As autistic symptoms are increased in individuals with 22q11.2 deletion syndrome, and large 22q11.2 deletions and duplications have been observed in ASD individuals, in this study, 98 individuals with ASD and 234 control individuals were genotyped for eight single-nucleotide polymorphisms in ADORA2A.]. 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:19565319
;
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:NP748252.RAzLE8no3PSWQnM4nNpCXLZEGwAOpvr1eZxSES2Fi8WZY130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:24+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:disgenetv3.0rdf
;
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" .
}