@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP744365.RAcYVxvmiGg98_nE5BGcXQ0Yb0HRZDYWHVtIHKnV1c5jA
> .
@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:NP744365.RAcYVxvmiGg98_nE5BGcXQ0Yb0HRZDYWHVtIHKnV1c5jA130_head
{
this:
np:hasAssertion
dgn-np:NP744365.RAcYVxvmiGg98_nE5BGcXQ0Yb0HRZDYWHVtIHKnV1c5jA130_assertion
;
np:hasProvenance
dgn-np:NP744365.RAcYVxvmiGg98_nE5BGcXQ0Yb0HRZDYWHVtIHKnV1c5jA130_provenance
;
np:hasPublicationInfo
dgn-np:NP744365.RAcYVxvmiGg98_nE5BGcXQ0Yb0HRZDYWHVtIHKnV1c5jA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP744365.RAcYVxvmiGg98_nE5BGcXQ0Yb0HRZDYWHVtIHKnV1c5jA130_assertion
a
np:Assertion
.
dgn-np:NP744365.RAcYVxvmiGg98_nE5BGcXQ0Yb0HRZDYWHVtIHKnV1c5jA130_provenance
a
np:Provenance
.
dgn-np:NP744365.RAcYVxvmiGg98_nE5BGcXQ0Yb0HRZDYWHVtIHKnV1c5jA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP744365.RAcYVxvmiGg98_nE5BGcXQ0Yb0HRZDYWHVtIHKnV1c5jA130_assertion
{
miriam-gene:1813
a
ncit:C16612
.
lld:C1328247
a
ncit:C7057
.
dgn-gda:DGN473b739ce5b2600de9267b3ffd65bdd5
sio:SIO_000628
miriam-gene:1813
,
lld:C1328247
;
a
sio:SIO_001121
.
}
dgn-np:NP744365.RAcYVxvmiGg98_nE5BGcXQ0Yb0HRZDYWHVtIHKnV1c5jA130_provenance
{
dgn-np:NP744365.RAcYVxvmiGg98_nE5BGcXQ0Yb0HRZDYWHVtIHKnV1c5jA130_assertion
dcterms:description
"[Our data are consistent with the hypothesis that DRD2 gene variants marked by these polymorphisms may work, probably in concert with other genetic and environmental factors, to enhance vulnerability to psychostimulant abuse.]. 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:8894071
;
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:NP744365.RAcYVxvmiGg98_nE5BGcXQ0Yb0HRZDYWHVtIHKnV1c5jA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:31+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" .
}