@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP555544.RA0N3XYUtfqZa3qWhQfCuogC6C1nZ_D1pOmKvjL6WzWww
> .
@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:NP555544.RA0N3XYUtfqZa3qWhQfCuogC6C1nZ_D1pOmKvjL6WzWww130_head
{
this:
np:hasAssertion
dgn-np:NP555544.RA0N3XYUtfqZa3qWhQfCuogC6C1nZ_D1pOmKvjL6WzWww130_assertion
;
np:hasProvenance
dgn-np:NP555544.RA0N3XYUtfqZa3qWhQfCuogC6C1nZ_D1pOmKvjL6WzWww130_provenance
;
np:hasPublicationInfo
dgn-np:NP555544.RA0N3XYUtfqZa3qWhQfCuogC6C1nZ_D1pOmKvjL6WzWww130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP555544.RA0N3XYUtfqZa3qWhQfCuogC6C1nZ_D1pOmKvjL6WzWww130_assertion
a
np:Assertion
.
dgn-np:NP555544.RA0N3XYUtfqZa3qWhQfCuogC6C1nZ_D1pOmKvjL6WzWww130_provenance
a
np:Provenance
.
dgn-np:NP555544.RA0N3XYUtfqZa3qWhQfCuogC6C1nZ_D1pOmKvjL6WzWww130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP555544.RA0N3XYUtfqZa3qWhQfCuogC6C1nZ_D1pOmKvjL6WzWww130_assertion
{
miriam-gene:1813
a
ncit:C16612
.
lld:C0011570
a
ncit:C7057
.
dgn-gda:DGNa065ba824733719e3b7389faf88e3ba4
sio:SIO_000628
miriam-gene:1813
,
lld:C0011570
;
a
sio:SIO_001121
.
}
dgn-np:NP555544.RA0N3XYUtfqZa3qWhQfCuogC6C1nZ_D1pOmKvjL6WzWww130_provenance
{
dgn-np:NP555544.RA0N3XYUtfqZa3qWhQfCuogC6C1nZ_D1pOmKvjL6WzWww130_assertion
dcterms:description
"[Because the D2 dopamine receptor (DRD2) A1 allele has been associated with alcoholism and other substance use disorders, negative affect, measured by the Beck Depression Inventory (BDI), was determined in four groups of children: boys and girls with the A1+ allele (A1A1 and A1A2 genotypes) and with the A1- allele (A2A2 genotype).]. 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:13679114
;
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:NP555544.RA0N3XYUtfqZa3qWhQfCuogC6C1nZ_D1pOmKvjL6WzWww130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:35+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" .
}