@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP520018.RAeW1Vi7zXAwM7wvfqB0ElZ876KaVqUgOAsaLkzzJN2uw
> .
@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:NP520018.RAeW1Vi7zXAwM7wvfqB0ElZ876KaVqUgOAsaLkzzJN2uw130_head
{
this:
np:hasAssertion
dgn-np:NP520018.RAeW1Vi7zXAwM7wvfqB0ElZ876KaVqUgOAsaLkzzJN2uw130_assertion
;
np:hasProvenance
dgn-np:NP520018.RAeW1Vi7zXAwM7wvfqB0ElZ876KaVqUgOAsaLkzzJN2uw130_provenance
;
np:hasPublicationInfo
dgn-np:NP520018.RAeW1Vi7zXAwM7wvfqB0ElZ876KaVqUgOAsaLkzzJN2uw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP520018.RAeW1Vi7zXAwM7wvfqB0ElZ876KaVqUgOAsaLkzzJN2uw130_assertion
a
np:Assertion
.
dgn-np:NP520018.RAeW1Vi7zXAwM7wvfqB0ElZ876KaVqUgOAsaLkzzJN2uw130_provenance
a
np:Provenance
.
dgn-np:NP520018.RAeW1Vi7zXAwM7wvfqB0ElZ876KaVqUgOAsaLkzzJN2uw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP520018.RAeW1Vi7zXAwM7wvfqB0ElZ876KaVqUgOAsaLkzzJN2uw130_assertion
{
miriam-gene:7517
a
ncit:C16612
.
lld:C1527249
a
ncit:C7057
.
dgn-gda:DGN5e6d0e6969a2ffe886af3f6780130b97
sio:SIO_000628
miriam-gene:7517
,
lld:C1527249
;
a
sio:SIO_001121
.
}
dgn-np:NP520018.RAeW1Vi7zXAwM7wvfqB0ElZ876KaVqUgOAsaLkzzJN2uw130_provenance
{
dgn-np:NP520018.RAeW1Vi7zXAwM7wvfqB0ElZ876KaVqUgOAsaLkzzJN2uw130_assertion
dcterms:description
"[The aim of this study was to investigate the associations between the APE1 Asp148Glu, hOGG1 Ser326Cys, XRCC1 Arg399Gln, XRCC3 Thr241Met, XPD Lys751Gln, XPG Asp1104His polymorphisms and CRC risk in Turkish population.]. 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:21561390
;
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:NP520018.RAeW1Vi7zXAwM7wvfqB0ElZ876KaVqUgOAsaLkzzJN2uw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:09+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" .
}