@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP59400.RAlxtFI08YfhWYnUYEIXAApWvi9GB01Tg7PyB3xVxSuMc
> .
@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:NP59400.RAlxtFI08YfhWYnUYEIXAApWvi9GB01Tg7PyB3xVxSuMc130_head
{
this:
np:hasAssertion
dgn-np:NP59400.RAlxtFI08YfhWYnUYEIXAApWvi9GB01Tg7PyB3xVxSuMc130_assertion
;
np:hasProvenance
dgn-np:NP59400.RAlxtFI08YfhWYnUYEIXAApWvi9GB01Tg7PyB3xVxSuMc130_provenance
;
np:hasPublicationInfo
dgn-np:NP59400.RAlxtFI08YfhWYnUYEIXAApWvi9GB01Tg7PyB3xVxSuMc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP59400.RAlxtFI08YfhWYnUYEIXAApWvi9GB01Tg7PyB3xVxSuMc130_assertion
a
np:Assertion
.
dgn-np:NP59400.RAlxtFI08YfhWYnUYEIXAApWvi9GB01Tg7PyB3xVxSuMc130_provenance
a
np:Provenance
.
dgn-np:NP59400.RAlxtFI08YfhWYnUYEIXAApWvi9GB01Tg7PyB3xVxSuMc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP59400.RAlxtFI08YfhWYnUYEIXAApWvi9GB01Tg7PyB3xVxSuMc130_assertion
{
miriam-gene:7515
a
ncit:C16612
.
lld:C0005684
a
ncit:C7057
.
dgn-gda:DGN4bf2db64781344bedef54dafa5c9915b
sio:SIO_000628
miriam-gene:7515
,
lld:C0005684
;
a
sio:SIO_001122
.
}
dgn-np:NP59400.RAlxtFI08YfhWYnUYEIXAApWvi9GB01Tg7PyB3xVxSuMc130_provenance
{
dgn-np:NP59400.RAlxtFI08YfhWYnUYEIXAApWvi9GB01Tg7PyB3xVxSuMc130_assertion
dcterms:description
"[It indicated that XRCC1 R399Q and R194W might not be risk factors to bladder cancer, but the 399QQ genotype decreased susceptibility of bladder cancer under recessive model and homozygote contrast among ever-smokers.]. 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:18765423
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP59400.RAlxtFI08YfhWYnUYEIXAApWvi9GB01Tg7PyB3xVxSuMc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:28+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" .
}