@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP168440.RA4UZW2XlgJZRrkqhaeEiMJGZQomRfKVgHDu1NDtqeEAI
> .
@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:NP168440.RA4UZW2XlgJZRrkqhaeEiMJGZQomRfKVgHDu1NDtqeEAI130_head
{
this:
np:hasAssertion
dgn-np:NP168440.RA4UZW2XlgJZRrkqhaeEiMJGZQomRfKVgHDu1NDtqeEAI130_assertion
;
np:hasProvenance
dgn-np:NP168440.RA4UZW2XlgJZRrkqhaeEiMJGZQomRfKVgHDu1NDtqeEAI130_provenance
;
np:hasPublicationInfo
dgn-np:NP168440.RA4UZW2XlgJZRrkqhaeEiMJGZQomRfKVgHDu1NDtqeEAI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP168440.RA4UZW2XlgJZRrkqhaeEiMJGZQomRfKVgHDu1NDtqeEAI130_assertion
a
np:Assertion
.
dgn-np:NP168440.RA4UZW2XlgJZRrkqhaeEiMJGZQomRfKVgHDu1NDtqeEAI130_provenance
a
np:Provenance
.
dgn-np:NP168440.RA4UZW2XlgJZRrkqhaeEiMJGZQomRfKVgHDu1NDtqeEAI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP168440.RA4UZW2XlgJZRrkqhaeEiMJGZQomRfKVgHDu1NDtqeEAI130_assertion
{
miriam-gene:57152
a
ncit:C16612
.
lld:C1263846
a
ncit:C7057
.
dgn-gda:DGN72898f93ce10dbbb30f9514132d87a5d
sio:SIO_000628
miriam-gene:57152
,
lld:C1263846
;
a
sio:SIO_001121
.
}
dgn-np:NP168440.RA4UZW2XlgJZRrkqhaeEiMJGZQomRfKVgHDu1NDtqeEAI130_provenance
{
dgn-np:NP168440.RA4UZW2XlgJZRrkqhaeEiMJGZQomRfKVgHDu1NDtqeEAI130_assertion
dcterms:description
"[In the ADHD patients, ANCOVA revealed that there were no significant differences in the subscales and total score between the ADHD probands with the CC genotype and those with the CG and GG genotypes in ARS and the Continuous Performance Test (CPT) when adjusting for age and gender.]. 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:20470849
;
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:NP168440.RA4UZW2XlgJZRrkqhaeEiMJGZQomRfKVgHDu1NDtqeEAI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:31+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" .
}