@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP705196.RAr6nGqxS6WsWfhgwFyerzzebzJVsBVsqpJoTTtCX265g
> .
@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:NP705196.RAr6nGqxS6WsWfhgwFyerzzebzJVsBVsqpJoTTtCX265g130_head
{
this:
np:hasAssertion
dgn-np:NP705196.RAr6nGqxS6WsWfhgwFyerzzebzJVsBVsqpJoTTtCX265g130_assertion
;
np:hasProvenance
dgn-np:NP705196.RAr6nGqxS6WsWfhgwFyerzzebzJVsBVsqpJoTTtCX265g130_provenance
;
np:hasPublicationInfo
dgn-np:NP705196.RAr6nGqxS6WsWfhgwFyerzzebzJVsBVsqpJoTTtCX265g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP705196.RAr6nGqxS6WsWfhgwFyerzzebzJVsBVsqpJoTTtCX265g130_assertion
a
np:Assertion
.
dgn-np:NP705196.RAr6nGqxS6WsWfhgwFyerzzebzJVsBVsqpJoTTtCX265g130_provenance
a
np:Provenance
.
dgn-np:NP705196.RAr6nGqxS6WsWfhgwFyerzzebzJVsBVsqpJoTTtCX265g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP705196.RAr6nGqxS6WsWfhgwFyerzzebzJVsBVsqpJoTTtCX265g130_assertion
{
miriam-gene:7515
a
ncit:C16612
.
lld:C0017168
a
ncit:C7057
.
dgn-gda:DGNcddbc8f34fd5c5fb5452bf8bb11cda65
sio:SIO_000628
miriam-gene:7515
,
lld:C0017168
;
a
sio:SIO_001121
.
}
dgn-np:NP705196.RAr6nGqxS6WsWfhgwFyerzzebzJVsBVsqpJoTTtCX265g130_provenance
{
dgn-np:NP705196.RAr6nGqxS6WsWfhgwFyerzzebzJVsBVsqpJoTTtCX265g130_assertion
dcterms:description
"[The protective effect of the homozygous variant of XRCC1 Arg399Gln for GERD and BE suggests that base excision repair alterations may occur early in progression to EADC, likely in response to GERD-induced endogenous oxidative or inflammatory DNA damage.]. 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:15878910
;
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:NP705196.RAr6nGqxS6WsWfhgwFyerzzebzJVsBVsqpJoTTtCX265g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:08+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" .
}