@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP653231.RA85ufjxUMZLp02N5JxdtUQbKmNDuXzEqBTmjm9dwDRuY
> .
@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:NP653231.RA85ufjxUMZLp02N5JxdtUQbKmNDuXzEqBTmjm9dwDRuY130_head
{
this:
np:hasAssertion
dgn-np:NP653231.RA85ufjxUMZLp02N5JxdtUQbKmNDuXzEqBTmjm9dwDRuY130_assertion
;
np:hasProvenance
dgn-np:NP653231.RA85ufjxUMZLp02N5JxdtUQbKmNDuXzEqBTmjm9dwDRuY130_provenance
;
np:hasPublicationInfo
dgn-np:NP653231.RA85ufjxUMZLp02N5JxdtUQbKmNDuXzEqBTmjm9dwDRuY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP653231.RA85ufjxUMZLp02N5JxdtUQbKmNDuXzEqBTmjm9dwDRuY130_assertion
a
np:Assertion
.
dgn-np:NP653231.RA85ufjxUMZLp02N5JxdtUQbKmNDuXzEqBTmjm9dwDRuY130_provenance
a
np:Provenance
.
dgn-np:NP653231.RA85ufjxUMZLp02N5JxdtUQbKmNDuXzEqBTmjm9dwDRuY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP653231.RA85ufjxUMZLp02N5JxdtUQbKmNDuXzEqBTmjm9dwDRuY130_assertion
{
miriam-gene:1815
a
ncit:C16612
.
lld:C0006012
a
ncit:C7057
.
dgn-gda:DGN010296b3e7ff6a92a16edb3d03da2faa
sio:SIO_000628
miriam-gene:1815
,
lld:C0006012
;
a
sio:SIO_001121
.
}
dgn-np:NP653231.RA85ufjxUMZLp02N5JxdtUQbKmNDuXzEqBTmjm9dwDRuY130_provenance
{
dgn-np:NP653231.RA85ufjxUMZLp02N5JxdtUQbKmNDuXzEqBTmjm9dwDRuY130_assertion
dcterms:description
"[Our findings suggest that volumetric abnormalities in the dorsolateral prefrontal cortex and cerebellum may represent an intermediate neuroanatomical phenotype between DRD4 genotype and the clinical expression of ADHD in adults, but only in ADHD subjects without comorbid BPD.]. 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:18951431
;
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:NP653231.RA85ufjxUMZLp02N5JxdtUQbKmNDuXzEqBTmjm9dwDRuY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:33+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" .
}