@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP423904.RAhfLVF_INO21Bo91nh8piogPi2rbB_Xj5rhqw48LxFoI
> .
@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:NP423904.RAhfLVF_INO21Bo91nh8piogPi2rbB_Xj5rhqw48LxFoI130_head
{
this:
np:hasAssertion
dgn-np:NP423904.RAhfLVF_INO21Bo91nh8piogPi2rbB_Xj5rhqw48LxFoI130_assertion
;
np:hasProvenance
dgn-np:NP423904.RAhfLVF_INO21Bo91nh8piogPi2rbB_Xj5rhqw48LxFoI130_provenance
;
np:hasPublicationInfo
dgn-np:NP423904.RAhfLVF_INO21Bo91nh8piogPi2rbB_Xj5rhqw48LxFoI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP423904.RAhfLVF_INO21Bo91nh8piogPi2rbB_Xj5rhqw48LxFoI130_assertion
a
np:Assertion
.
dgn-np:NP423904.RAhfLVF_INO21Bo91nh8piogPi2rbB_Xj5rhqw48LxFoI130_provenance
a
np:Provenance
.
dgn-np:NP423904.RAhfLVF_INO21Bo91nh8piogPi2rbB_Xj5rhqw48LxFoI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP423904.RAhfLVF_INO21Bo91nh8piogPi2rbB_Xj5rhqw48LxFoI130_assertion
{
miriam-gene:5173
a
ncit:C16612
.
lld:C0013146
a
ncit:C7057
.
dgn-gda:DGN987c1e491f019a12d1f30aa858539417
sio:SIO_000628
miriam-gene:5173
,
lld:C0013146
;
a
sio:SIO_001121
.
}
dgn-np:NP423904.RAhfLVF_INO21Bo91nh8piogPi2rbB_Xj5rhqw48LxFoI130_provenance
{
dgn-np:NP423904.RAhfLVF_INO21Bo91nh8piogPi2rbB_Xj5rhqw48LxFoI130_assertion
dcterms:description
"[Our results suggest that this allelic variation at the promoter region of the prodynorphin gene (alleles with three or four repeats), which may result in enhanced transcription of the gene, may contribute to relative protection and decrease individual vulnerability to develop cocaine dependence or 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:11992566
;
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:NP423904.RAhfLVF_INO21Bo91nh8piogPi2rbB_Xj5rhqw48LxFoI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:11+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" .
}