@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP227833.RAcRoWKZdp5t-hcRJEZ3aT1Kt1yV552BCi7AafoI9HQMc
> .
@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:NP227833.RAcRoWKZdp5t-hcRJEZ3aT1Kt1yV552BCi7AafoI9HQMc130_head
{
this:
np:hasAssertion
dgn-np:NP227833.RAcRoWKZdp5t-hcRJEZ3aT1Kt1yV552BCi7AafoI9HQMc130_assertion
;
np:hasProvenance
dgn-np:NP227833.RAcRoWKZdp5t-hcRJEZ3aT1Kt1yV552BCi7AafoI9HQMc130_provenance
;
np:hasPublicationInfo
dgn-np:NP227833.RAcRoWKZdp5t-hcRJEZ3aT1Kt1yV552BCi7AafoI9HQMc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP227833.RAcRoWKZdp5t-hcRJEZ3aT1Kt1yV552BCi7AafoI9HQMc130_assertion
a
np:Assertion
.
dgn-np:NP227833.RAcRoWKZdp5t-hcRJEZ3aT1Kt1yV552BCi7AafoI9HQMc130_provenance
a
np:Provenance
.
dgn-np:NP227833.RAcRoWKZdp5t-hcRJEZ3aT1Kt1yV552BCi7AafoI9HQMc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP227833.RAcRoWKZdp5t-hcRJEZ3aT1Kt1yV552BCi7AafoI9HQMc130_assertion
{
miriam-gene:7515
a
ncit:C16612
.
lld:C0025209
a
ncit:C7057
.
dgn-gda:DGN4982948f4ada9fe5a6761f5b215519f6
sio:SIO_000628
miriam-gene:7515
,
lld:C0025209
;
a
sio:SIO_001121
.
}
dgn-np:NP227833.RAcRoWKZdp5t-hcRJEZ3aT1Kt1yV552BCi7AafoI9HQMc130_provenance
{
dgn-np:NP227833.RAcRoWKZdp5t-hcRJEZ3aT1Kt1yV552BCi7AafoI9HQMc130_assertion
dcterms:description
"[Data from a case-control study of 792 cases and 792 matched controls conducted in Bangladesh from 2001 to 2003 were analyzed using conditional logistic regression to assess the associations between four common base excision repair (BER) genetic polymorphisms X-ray repair cross-complementing group 1 (XRCC1) Arg399Gln, XRCC1 Arg194Trp, human 8-oxoguanine DNA glycosylase (hOGG1) Ser326Cys and apurinic/apyrimidinic endonuclease (APE1) Asp148Glu and arsenic-induced skin lesions including melanosis and keratosis.]. 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:17374727
;
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:NP227833.RAcRoWKZdp5t-hcRJEZ3aT1Kt1yV552BCi7AafoI9HQMc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:06+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" .
}