@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP67713.RAl4FoGQk0tKu21TG6dsFgi_kbL2o2AfQdg52TKoxZJSg
> .
@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:NP67713.RAl4FoGQk0tKu21TG6dsFgi_kbL2o2AfQdg52TKoxZJSg130_head
{
this:
np:hasAssertion
dgn-np:NP67713.RAl4FoGQk0tKu21TG6dsFgi_kbL2o2AfQdg52TKoxZJSg130_assertion
;
np:hasProvenance
dgn-np:NP67713.RAl4FoGQk0tKu21TG6dsFgi_kbL2o2AfQdg52TKoxZJSg130_provenance
;
np:hasPublicationInfo
dgn-np:NP67713.RAl4FoGQk0tKu21TG6dsFgi_kbL2o2AfQdg52TKoxZJSg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP67713.RAl4FoGQk0tKu21TG6dsFgi_kbL2o2AfQdg52TKoxZJSg130_assertion
a
np:Assertion
.
dgn-np:NP67713.RAl4FoGQk0tKu21TG6dsFgi_kbL2o2AfQdg52TKoxZJSg130_provenance
a
np:Provenance
.
dgn-np:NP67713.RAl4FoGQk0tKu21TG6dsFgi_kbL2o2AfQdg52TKoxZJSg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP67713.RAl4FoGQk0tKu21TG6dsFgi_kbL2o2AfQdg52TKoxZJSg130_assertion
{
miriam-gene:11122
a
ncit:C16612
.
lld:C0040336
a
ncit:C7057
.
dgn-gda:DGN43e82e328b979663291b16481c25c3f6
sio:SIO_000628
miriam-gene:11122
,
lld:C0040336
;
a
sio:SIO_001122
.
}
dgn-np:NP67713.RAl4FoGQk0tKu21TG6dsFgi_kbL2o2AfQdg52TKoxZJSg130_provenance
{
dgn-np:NP67713.RAl4FoGQk0tKu21TG6dsFgi_kbL2o2AfQdg52TKoxZJSg130_assertion
dcterms:description
"[These results support polygenic genetics for success in abstaining from smoking, overlap with genetics of substance dependence and memory, and nominate gene variants for selective influences on therapeutic responses to bupropion vs NRT.]. 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:18519826
;
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:NP67713.RAl4FoGQk0tKu21TG6dsFgi_kbL2o2AfQdg52TKoxZJSg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:32+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" .
}