@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP99454.RAXk97uGrhoOu7EPOVK7A9zD5TCyrSo0ogIG6e_tW4XnY
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP99454.RAXk97uGrhoOu7EPOVK7A9zD5TCyrSo0ogIG6e_tW4XnY130_head
{
this:
np:hasAssertion
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;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP99454.RAXk97uGrhoOu7EPOVK7A9zD5TCyrSo0ogIG6e_tW4XnY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP99454.RAXk97uGrhoOu7EPOVK7A9zD5TCyrSo0ogIG6e_tW4XnY130_assertion
a
np:Assertion
.
dgn-np:NP99454.RAXk97uGrhoOu7EPOVK7A9zD5TCyrSo0ogIG6e_tW4XnY130_provenance
a
np:Provenance
.
dgn-np:NP99454.RAXk97uGrhoOu7EPOVK7A9zD5TCyrSo0ogIG6e_tW4XnY130_publicationInfo
a
np:PublicationInfo
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{
miriam-gene:7508
a
ncit:C16612
.
lld:C0005684
a
ncit:C7057
.
dgn-gda:DGN83f45e3ad34e782591bd93d40be582ce
sio:SIO_000628
miriam-gene:7508
,
lld:C0005684
;
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sio:SIO_001122
.
}
dgn-np:NP99454.RAXk97uGrhoOu7EPOVK7A9zD5TCyrSo0ogIG6e_tW4XnY130_provenance
{
dgn-np:NP99454.RAXk97uGrhoOu7EPOVK7A9zD5TCyrSo0ogIG6e_tW4XnY130_assertion
dcterms:description
"[We evaluated the influence of common genetic variation in the NER pathway on bladder cancer risk by analyzing 22 single nucleotide polymorphisms (SNP) in seven NER genes (XPC, RAD23B, ERCC1, ERCC2, ERCC4, ERCC5, and ERCC6).]. 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:16537713
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP99454.RAXk97uGrhoOu7EPOVK7A9zD5TCyrSo0ogIG6e_tW4XnY130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:42:33+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
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;
pav:authoredBy
<
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> , <
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> , <
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
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