@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP799648.RADgNJ2h3uG3sGfDFtqe1-FpbyAaAdYDiGNKNVZpl2R1o
> .
@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:NP799648.RADgNJ2h3uG3sGfDFtqe1-FpbyAaAdYDiGNKNVZpl2R1o130_head
{
this:
np:hasAssertion
dgn-np:NP799648.RADgNJ2h3uG3sGfDFtqe1-FpbyAaAdYDiGNKNVZpl2R1o130_assertion
;
np:hasProvenance
dgn-np:NP799648.RADgNJ2h3uG3sGfDFtqe1-FpbyAaAdYDiGNKNVZpl2R1o130_provenance
;
np:hasPublicationInfo
dgn-np:NP799648.RADgNJ2h3uG3sGfDFtqe1-FpbyAaAdYDiGNKNVZpl2R1o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP799648.RADgNJ2h3uG3sGfDFtqe1-FpbyAaAdYDiGNKNVZpl2R1o130_assertion
a
np:Assertion
.
dgn-np:NP799648.RADgNJ2h3uG3sGfDFtqe1-FpbyAaAdYDiGNKNVZpl2R1o130_provenance
a
np:Provenance
.
dgn-np:NP799648.RADgNJ2h3uG3sGfDFtqe1-FpbyAaAdYDiGNKNVZpl2R1o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP799648.RADgNJ2h3uG3sGfDFtqe1-FpbyAaAdYDiGNKNVZpl2R1o130_assertion
{
miriam-gene:7515
a
ncit:C16612
.
lld:C2316810
a
ncit:C7057
.
dgn-gda:DGN2d34554761a93da7a83a6bfe7ddbf587
sio:SIO_000628
miriam-gene:7515
,
lld:C2316810
;
a
sio:SIO_001121
.
}
dgn-np:NP799648.RADgNJ2h3uG3sGfDFtqe1-FpbyAaAdYDiGNKNVZpl2R1o130_provenance
{
dgn-np:NP799648.RADgNJ2h3uG3sGfDFtqe1-FpbyAaAdYDiGNKNVZpl2R1o130_assertion
dcterms:description
"[This is the first report showing an association between DNA repair gene polymorphisms and ESRD development, and suggests that XRCC1 Arg399Gln polymorphism may confer increased risk for the development of the disease.]. 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:22302399
;
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:NP799648.RADgNJ2h3uG3sGfDFtqe1-FpbyAaAdYDiGNKNVZpl2R1o130_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" .
}