@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP482127.RAfeVRSN22IDE4icP-g1r1WWm5Kim_LZgAtZiV9bTjZ4g
> .
@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:NP482127.RAfeVRSN22IDE4icP-g1r1WWm5Kim_LZgAtZiV9bTjZ4g130_head
{
this:
np:hasAssertion
dgn-np:NP482127.RAfeVRSN22IDE4icP-g1r1WWm5Kim_LZgAtZiV9bTjZ4g130_assertion
;
np:hasProvenance
dgn-np:NP482127.RAfeVRSN22IDE4icP-g1r1WWm5Kim_LZgAtZiV9bTjZ4g130_provenance
;
np:hasPublicationInfo
dgn-np:NP482127.RAfeVRSN22IDE4icP-g1r1WWm5Kim_LZgAtZiV9bTjZ4g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP482127.RAfeVRSN22IDE4icP-g1r1WWm5Kim_LZgAtZiV9bTjZ4g130_assertion
a
np:Assertion
.
dgn-np:NP482127.RAfeVRSN22IDE4icP-g1r1WWm5Kim_LZgAtZiV9bTjZ4g130_provenance
a
np:Provenance
.
dgn-np:NP482127.RAfeVRSN22IDE4icP-g1r1WWm5Kim_LZgAtZiV9bTjZ4g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP482127.RAfeVRSN22IDE4icP-g1r1WWm5Kim_LZgAtZiV9bTjZ4g130_assertion
{
miriam-gene:4810
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGNab0ce61ad3f3faffa4a8a0e4cf3d6357
sio:SIO_000628
miriam-gene:4810
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP482127.RAfeVRSN22IDE4icP-g1r1WWm5Kim_LZgAtZiV9bTjZ4g130_provenance
{
dgn-np:NP482127.RAfeVRSN22IDE4icP-g1r1WWm5Kim_LZgAtZiV9bTjZ4g130_assertion
dcterms:description
"[The contribution of common genetic variation to one or more established smoking behaviors was investigated in a joint analysis of two genome wide association studies (GWAS) performed as part of the Cancer Genetic Markers of Susceptibility (CGEMS) project in 2,329 men from the Prostate, Lung, Colon and Ovarian (PLCO) Trial, and 2,282 women from the Nurses' Health Study (NHS).]. 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:19247474
;
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:NP482127.RAfeVRSN22IDE4icP-g1r1WWm5Kim_LZgAtZiV9bTjZ4g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:48+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" .
}