@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP201993.RASxy8k3QJ3hJr_XpQc5VJmRqveJPZy4QFOndbSQLS2N8
> .
@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:NP201993.RASxy8k3QJ3hJr_XpQc5VJmRqveJPZy4QFOndbSQLS2N8130_head
{
this:
np:hasAssertion
dgn-np:NP201993.RASxy8k3QJ3hJr_XpQc5VJmRqveJPZy4QFOndbSQLS2N8130_assertion
;
np:hasProvenance
dgn-np:NP201993.RASxy8k3QJ3hJr_XpQc5VJmRqveJPZy4QFOndbSQLS2N8130_provenance
;
np:hasPublicationInfo
dgn-np:NP201993.RASxy8k3QJ3hJr_XpQc5VJmRqveJPZy4QFOndbSQLS2N8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP201993.RASxy8k3QJ3hJr_XpQc5VJmRqveJPZy4QFOndbSQLS2N8130_assertion
a
np:Assertion
.
dgn-np:NP201993.RASxy8k3QJ3hJr_XpQc5VJmRqveJPZy4QFOndbSQLS2N8130_provenance
a
np:Provenance
.
dgn-np:NP201993.RASxy8k3QJ3hJr_XpQc5VJmRqveJPZy4QFOndbSQLS2N8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP201993.RASxy8k3QJ3hJr_XpQc5VJmRqveJPZy4QFOndbSQLS2N8130_assertion
{
miriam-gene:1815
a
ncit:C16612
.
lld:C1263846
a
ncit:C7057
.
dgn-gda:DGNf7c657c94a4cb75522d0d90dbec1ad4b
sio:SIO_000628
miriam-gene:1815
,
lld:C1263846
;
a
sio:SIO_001121
.
}
dgn-np:NP201993.RASxy8k3QJ3hJr_XpQc5VJmRqveJPZy4QFOndbSQLS2N8130_provenance
{
dgn-np:NP201993.RASxy8k3QJ3hJr_XpQc5VJmRqveJPZy4QFOndbSQLS2N8130_assertion
dcterms:description
"[It is now established that certain alleles of the genes coding for the dopamine D4 receptor and the dopamine transporter occur more frequently in children with ADHD than in healthy controls, and we are finding other DNA changes associated with ADHD.]. 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:16055819
;
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:NP201993.RASxy8k3QJ3hJr_XpQc5VJmRqveJPZy4QFOndbSQLS2N8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:51+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" .
}