@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP799133.RAmG-TrXK4xZoR1WI4QpG467RB8Zp29T5AWxml448NZc4
> .
@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:NP799133.RAmG-TrXK4xZoR1WI4QpG467RB8Zp29T5AWxml448NZc4130_head
{
this:
np:hasAssertion
dgn-np:NP799133.RAmG-TrXK4xZoR1WI4QpG467RB8Zp29T5AWxml448NZc4130_assertion
;
np:hasProvenance
dgn-np:NP799133.RAmG-TrXK4xZoR1WI4QpG467RB8Zp29T5AWxml448NZc4130_provenance
;
np:hasPublicationInfo
dgn-np:NP799133.RAmG-TrXK4xZoR1WI4QpG467RB8Zp29T5AWxml448NZc4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP799133.RAmG-TrXK4xZoR1WI4QpG467RB8Zp29T5AWxml448NZc4130_assertion
a
np:Assertion
.
dgn-np:NP799133.RAmG-TrXK4xZoR1WI4QpG467RB8Zp29T5AWxml448NZc4130_provenance
a
np:Provenance
.
dgn-np:NP799133.RAmG-TrXK4xZoR1WI4QpG467RB8Zp29T5AWxml448NZc4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP799133.RAmG-TrXK4xZoR1WI4QpG467RB8Zp29T5AWxml448NZc4130_assertion
{
miriam-gene:4780
a
ncit:C16612
.
lld:C0242379
a
ncit:C7057
.
dgn-gda:DGN5affc0b935f47371f6e247c6bd6edd58
sio:SIO_000628
miriam-gene:4780
,
lld:C0242379
;
a
sio:SIO_001121
.
}
dgn-np:NP799133.RAmG-TrXK4xZoR1WI4QpG467RB8Zp29T5AWxml448NZc4130_provenance
{
dgn-np:NP799133.RAmG-TrXK4xZoR1WI4QpG467RB8Zp29T5AWxml448NZc4130_assertion
dcterms:description
"[In excellent agreement with this finding, we found that minor A/A homozygotes of a single nucleotide polymorphism (SNP) in the human NRF2 upstream promoter region (rs6721961) exhibited significantly diminished NRF2 gene expression and, consequently, an increased risk of lung cancer, especially those who had ever smoked.]. 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:23572560
;
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:NP799133.RAmG-TrXK4xZoR1WI4QpG467RB8Zp29T5AWxml448NZc4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:10+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" .
}