@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP189277.RAyIec9EVvaOIQjY-M1PwGNAPIRrcXT1x4wksxo_1hCqg
> .
@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:NP189277.RAyIec9EVvaOIQjY-M1PwGNAPIRrcXT1x4wksxo_1hCqg130_head
{
this:
np:hasAssertion
dgn-np:NP189277.RAyIec9EVvaOIQjY-M1PwGNAPIRrcXT1x4wksxo_1hCqg130_assertion
;
np:hasProvenance
dgn-np:NP189277.RAyIec9EVvaOIQjY-M1PwGNAPIRrcXT1x4wksxo_1hCqg130_provenance
;
np:hasPublicationInfo
dgn-np:NP189277.RAyIec9EVvaOIQjY-M1PwGNAPIRrcXT1x4wksxo_1hCqg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP189277.RAyIec9EVvaOIQjY-M1PwGNAPIRrcXT1x4wksxo_1hCqg130_assertion
a
np:Assertion
.
dgn-np:NP189277.RAyIec9EVvaOIQjY-M1PwGNAPIRrcXT1x4wksxo_1hCqg130_provenance
a
np:Provenance
.
dgn-np:NP189277.RAyIec9EVvaOIQjY-M1PwGNAPIRrcXT1x4wksxo_1hCqg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP189277.RAyIec9EVvaOIQjY-M1PwGNAPIRrcXT1x4wksxo_1hCqg130_assertion
{
miriam-gene:4968
a
ncit:C16612
.
lld:C0030567
a
ncit:C7057
.
dgn-gda:DGN00fce0ddc567b6c0ac381fa6c928f468
sio:SIO_000628
miriam-gene:4968
,
lld:C0030567
;
a
sio:SIO_001121
.
}
dgn-np:NP189277.RAyIec9EVvaOIQjY-M1PwGNAPIRrcXT1x4wksxo_1hCqg130_provenance
{
dgn-np:NP189277.RAyIec9EVvaOIQjY-M1PwGNAPIRrcXT1x4wksxo_1hCqg130_assertion
dcterms:description
"[In the light of these findings, we investigated whether DNA repair gene polymorphisms (XRCC1 Arg399Gln, XRCC3 Thr241Met XPD Lys751Gln, XPG Asp1104His, APE1 Asp148Glu, and HOGG1 Ser326Cys) account for an increased risk of Parkinson's disease (PD).]. 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:22224629
;
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:NP189277.RAyIec9EVvaOIQjY-M1PwGNAPIRrcXT1x4wksxo_1hCqg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:44+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" .
}