@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP77039.RAFrHIfSIoMKdN3ronfVrTX9fpCGcrB9Pnutcoed0AO8I
> .
@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:NP77039.RAFrHIfSIoMKdN3ronfVrTX9fpCGcrB9Pnutcoed0AO8I130_head
{
this:
np:hasAssertion
dgn-np:NP77039.RAFrHIfSIoMKdN3ronfVrTX9fpCGcrB9Pnutcoed0AO8I130_assertion
;
np:hasProvenance
dgn-np:NP77039.RAFrHIfSIoMKdN3ronfVrTX9fpCGcrB9Pnutcoed0AO8I130_provenance
;
np:hasPublicationInfo
dgn-np:NP77039.RAFrHIfSIoMKdN3ronfVrTX9fpCGcrB9Pnutcoed0AO8I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP77039.RAFrHIfSIoMKdN3ronfVrTX9fpCGcrB9Pnutcoed0AO8I130_assertion
a
np:Assertion
.
dgn-np:NP77039.RAFrHIfSIoMKdN3ronfVrTX9fpCGcrB9Pnutcoed0AO8I130_provenance
a
np:Provenance
.
dgn-np:NP77039.RAFrHIfSIoMKdN3ronfVrTX9fpCGcrB9Pnutcoed0AO8I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP77039.RAFrHIfSIoMKdN3ronfVrTX9fpCGcrB9Pnutcoed0AO8I130_assertion
{
miriam-gene:79817
a
ncit:C16612
.
lld:C0040336
a
ncit:C7057
.
dgn-gda:DGNf56f866414823fb4737ec1adb24e5148
sio:SIO_000628
miriam-gene:79817
,
lld:C0040336
;
a
sio:SIO_001122
.
}
dgn-np:NP77039.RAFrHIfSIoMKdN3ronfVrTX9fpCGcrB9Pnutcoed0AO8I130_provenance
{
dgn-np:NP77039.RAFrHIfSIoMKdN3ronfVrTX9fpCGcrB9Pnutcoed0AO8I130_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:NP77039.RAFrHIfSIoMKdN3ronfVrTX9fpCGcrB9Pnutcoed0AO8I130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:37+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" .
}