@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP83774.RAPgccNhteyeiA3CbDyB4iW1Xiqkf-BFCuW1FXzf7rLbg
> .
@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:NP83774.RAPgccNhteyeiA3CbDyB4iW1Xiqkf-BFCuW1FXzf7rLbg130_head
{
this:
np:hasAssertion
dgn-np:NP83774.RAPgccNhteyeiA3CbDyB4iW1Xiqkf-BFCuW1FXzf7rLbg130_assertion
;
np:hasProvenance
dgn-np:NP83774.RAPgccNhteyeiA3CbDyB4iW1Xiqkf-BFCuW1FXzf7rLbg130_provenance
;
np:hasPublicationInfo
dgn-np:NP83774.RAPgccNhteyeiA3CbDyB4iW1Xiqkf-BFCuW1FXzf7rLbg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP83774.RAPgccNhteyeiA3CbDyB4iW1Xiqkf-BFCuW1FXzf7rLbg130_assertion
a
np:Assertion
.
dgn-np:NP83774.RAPgccNhteyeiA3CbDyB4iW1Xiqkf-BFCuW1FXzf7rLbg130_provenance
a
np:Provenance
.
dgn-np:NP83774.RAPgccNhteyeiA3CbDyB4iW1Xiqkf-BFCuW1FXzf7rLbg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP83774.RAPgccNhteyeiA3CbDyB4iW1Xiqkf-BFCuW1FXzf7rLbg130_assertion
{
miriam-gene:4852
a
ncit:C16612
.
lld:C0236733
a
ncit:C7057
.
dgn-gda:DGN493b2884c45a7d541da780448f3831f3
sio:SIO_000628
miriam-gene:4852
,
lld:C0236733
;
a
sio:SIO_001122
.
}
dgn-np:NP83774.RAPgccNhteyeiA3CbDyB4iW1Xiqkf-BFCuW1FXzf7rLbg130_provenance
{
dgn-np:NP83774.RAPgccNhteyeiA3CbDyB4iW1Xiqkf-BFCuW1FXzf7rLbg130_assertion
dcterms:description
"[It is possible that genetic variants of the NPY1R gene affect the NPY-NPY receptor type Y1 signaling system in the brain, which may result in susceptibility to methamphetamine dependence or the development of methamphetamine psychosis, but the present findings need to be confirmed on replication.]. 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:19566775
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP83774.RAPgccNhteyeiA3CbDyB4iW1Xiqkf-BFCuW1FXzf7rLbg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:41+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" .
}