@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP904465.RADdOdIrfbS873moqCWFR2fd9Lur5HK9UMtuByZLWdFGY
> .
@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:NP904465.RADdOdIrfbS873moqCWFR2fd9Lur5HK9UMtuByZLWdFGY130_head
{
this:
np:hasAssertion
dgn-np:NP904465.RADdOdIrfbS873moqCWFR2fd9Lur5HK9UMtuByZLWdFGY130_assertion
;
np:hasProvenance
dgn-np:NP904465.RADdOdIrfbS873moqCWFR2fd9Lur5HK9UMtuByZLWdFGY130_provenance
;
np:hasPublicationInfo
dgn-np:NP904465.RADdOdIrfbS873moqCWFR2fd9Lur5HK9UMtuByZLWdFGY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP904465.RADdOdIrfbS873moqCWFR2fd9Lur5HK9UMtuByZLWdFGY130_assertion
a
np:Assertion
.
dgn-np:NP904465.RADdOdIrfbS873moqCWFR2fd9Lur5HK9UMtuByZLWdFGY130_provenance
a
np:Provenance
.
dgn-np:NP904465.RADdOdIrfbS873moqCWFR2fd9Lur5HK9UMtuByZLWdFGY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP904465.RADdOdIrfbS873moqCWFR2fd9Lur5HK9UMtuByZLWdFGY130_assertion
{
miriam-gene:133482
a
ncit:C16612
.
lld:C0220641
a
ncit:C7057
.
dgn-gda:DGN452c32dd739dff669a84a9cb565ebfe2
sio:SIO_000628
miriam-gene:133482
,
lld:C0220641
;
a
sio:SIO_001121
.
}
dgn-np:NP904465.RADdOdIrfbS873moqCWFR2fd9Lur5HK9UMtuByZLWdFGY130_provenance
{
dgn-np:NP904465.RADdOdIrfbS873moqCWFR2fd9Lur5HK9UMtuByZLWdFGY130_assertion
dcterms:description
"[A mini-case-control study with very small sample size showed no marked increase in the risk of developing oral cancer as the frequencies of the studied GST genotypes did not show any statistical significance.]. 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:19718946
;
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:NP904465.RADdOdIrfbS873moqCWFR2fd9Lur5HK9UMtuByZLWdFGY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:15+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" .
}