@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP463876.RAnL4iVXx8O6KiJjaS55bpqHhv1yQKGTp8HBxWqZ9QsbY
> .
@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:NP463876.RAnL4iVXx8O6KiJjaS55bpqHhv1yQKGTp8HBxWqZ9QsbY130_head
{
this:
np:hasAssertion
dgn-np:NP463876.RAnL4iVXx8O6KiJjaS55bpqHhv1yQKGTp8HBxWqZ9QsbY130_assertion
;
np:hasProvenance
dgn-np:NP463876.RAnL4iVXx8O6KiJjaS55bpqHhv1yQKGTp8HBxWqZ9QsbY130_provenance
;
np:hasPublicationInfo
dgn-np:NP463876.RAnL4iVXx8O6KiJjaS55bpqHhv1yQKGTp8HBxWqZ9QsbY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP463876.RAnL4iVXx8O6KiJjaS55bpqHhv1yQKGTp8HBxWqZ9QsbY130_assertion
a
np:Assertion
.
dgn-np:NP463876.RAnL4iVXx8O6KiJjaS55bpqHhv1yQKGTp8HBxWqZ9QsbY130_provenance
a
np:Provenance
.
dgn-np:NP463876.RAnL4iVXx8O6KiJjaS55bpqHhv1yQKGTp8HBxWqZ9QsbY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP463876.RAnL4iVXx8O6KiJjaS55bpqHhv1yQKGTp8HBxWqZ9QsbY130_assertion
{
miriam-gene:140809
a
ncit:C16612
.
lld:C0678222
a
ncit:C7057
.
dgn-gda:DGN65eabb5f51624b09d4e82095d616b9b5
sio:SIO_000628
miriam-gene:140809
,
lld:C0678222
;
a
sio:SIO_001121
.
}
dgn-np:NP463876.RAnL4iVXx8O6KiJjaS55bpqHhv1yQKGTp8HBxWqZ9QsbY130_provenance
{
dgn-np:NP463876.RAnL4iVXx8O6KiJjaS55bpqHhv1yQKGTp8HBxWqZ9QsbY130_assertion
dcterms:description
"[NRF2 and SRXN1 genetic polymorphisms are associated with breast cancer risk and survival, implicating that mechanisms associated with reactive oxygen species and NRF2 pathway are involved in breast cancer initiation and progression.]. 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:22964583
;
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:NP463876.RAnL4iVXx8O6KiJjaS55bpqHhv1yQKGTp8HBxWqZ9QsbY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:36+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" .
}