@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP872678.RAspcXFRhvWSi_wfqJjXaFKIlVvtrfN_ru-8mut7q1ZKI
> .
@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:NP872678.RAspcXFRhvWSi_wfqJjXaFKIlVvtrfN_ru-8mut7q1ZKI130_head
{
this:
np:hasAssertion
dgn-np:NP872678.RAspcXFRhvWSi_wfqJjXaFKIlVvtrfN_ru-8mut7q1ZKI130_assertion
;
np:hasProvenance
dgn-np:NP872678.RAspcXFRhvWSi_wfqJjXaFKIlVvtrfN_ru-8mut7q1ZKI130_provenance
;
np:hasPublicationInfo
dgn-np:NP872678.RAspcXFRhvWSi_wfqJjXaFKIlVvtrfN_ru-8mut7q1ZKI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP872678.RAspcXFRhvWSi_wfqJjXaFKIlVvtrfN_ru-8mut7q1ZKI130_assertion
a
np:Assertion
.
dgn-np:NP872678.RAspcXFRhvWSi_wfqJjXaFKIlVvtrfN_ru-8mut7q1ZKI130_provenance
a
np:Provenance
.
dgn-np:NP872678.RAspcXFRhvWSi_wfqJjXaFKIlVvtrfN_ru-8mut7q1ZKI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP872678.RAspcXFRhvWSi_wfqJjXaFKIlVvtrfN_ru-8mut7q1ZKI130_assertion
{
miriam-gene:2903
a
ncit:C16612
.
lld:C1263846
a
ncit:C7057
.
dgn-gda:DGNe0f922209650cd4fa2cec945c61f15ee
sio:SIO_000628
miriam-gene:2903
,
lld:C1263846
;
a
sio:SIO_001121
.
}
dgn-np:NP872678.RAspcXFRhvWSi_wfqJjXaFKIlVvtrfN_ru-8mut7q1ZKI130_provenance
{
dgn-np:NP872678.RAspcXFRhvWSi_wfqJjXaFKIlVvtrfN_ru-8mut7q1ZKI130_assertion
dcterms:description
"[Our data suggest that genetic variation in GRIN2A may confer increased risk for ADHD and that this, at least in part, might be responsible for the linkage result on 16p reported by Smalley et al.]. 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:14966475
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
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:NP872678.RAspcXFRhvWSi_wfqJjXaFKIlVvtrfN_ru-8mut7q1ZKI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:53+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" .
}