@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP848525.RAn25wDVyYheWOJheqDjnFSve9y-9qFk7VS4gpSWPxLJU
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP848525.RAn25wDVyYheWOJheqDjnFSve9y-9qFk7VS4gpSWPxLJU130_assertion
;
np:hasProvenance
dgn-np:NP848525.RAn25wDVyYheWOJheqDjnFSve9y-9qFk7VS4gpSWPxLJU130_provenance
;
np:hasPublicationInfo
dgn-np:NP848525.RAn25wDVyYheWOJheqDjnFSve9y-9qFk7VS4gpSWPxLJU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP848525.RAn25wDVyYheWOJheqDjnFSve9y-9qFk7VS4gpSWPxLJU130_assertion
a
np:Assertion
.
dgn-np:NP848525.RAn25wDVyYheWOJheqDjnFSve9y-9qFk7VS4gpSWPxLJU130_provenance
a
np:Provenance
.
dgn-np:NP848525.RAn25wDVyYheWOJheqDjnFSve9y-9qFk7VS4gpSWPxLJU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP848525.RAn25wDVyYheWOJheqDjnFSve9y-9qFk7VS4gpSWPxLJU130_assertion
{
miriam-gene:1813
a
ncit:C16612
.
lld:C0040332
a
ncit:C7057
.
dgn-gda:DGN82a98b29b168a718b1d65ed767680cd3
sio:SIO_000628
miriam-gene:1813
,
lld:C0040332
;
a
sio:SIO_001121
.
}
dgn-np:NP848525.RAn25wDVyYheWOJheqDjnFSve9y-9qFk7VS4gpSWPxLJU130_provenance
{
dgn-np:NP848525.RAn25wDVyYheWOJheqDjnFSve9y-9qFk7VS4gpSWPxLJU130_assertion
dcterms:description
"[Studies examining the role of genetic variability in modulating individual response to nicotine in humans have increased, with recent work showing that genetic variation at the dopamine D2 receptor (DRD2) predicts response to pharmacotherapy for tobacco dependence.]. 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:16896957
;
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:NP848525.RAn25wDVyYheWOJheqDjnFSve9y-9qFk7VS4gpSWPxLJU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:38+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" .
}