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http://rdf.disgenet.org/nanopublications.trig#NP247076.RAAowuyaCVCcrbtHd9_M0CJ2s2oH7SZpcoaX_jdWStWz8
> .
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http://www.w3.org/2000/01/rdf-schema#
> .
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http://www.w3.org/2001/XMLSchema#
> .
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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#
> .
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http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP247076.RAAowuyaCVCcrbtHd9_M0CJ2s2oH7SZpcoaX_jdWStWz8130_head
{
this:
np:hasAssertion
dgn-np:NP247076.RAAowuyaCVCcrbtHd9_M0CJ2s2oH7SZpcoaX_jdWStWz8130_assertion
;
np:hasProvenance
dgn-np:NP247076.RAAowuyaCVCcrbtHd9_M0CJ2s2oH7SZpcoaX_jdWStWz8130_provenance
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np:hasPublicationInfo
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;
a
np:Nanopublication
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dgn-np:NP247076.RAAowuyaCVCcrbtHd9_M0CJ2s2oH7SZpcoaX_jdWStWz8130_assertion
a
np:Assertion
.
dgn-np:NP247076.RAAowuyaCVCcrbtHd9_M0CJ2s2oH7SZpcoaX_jdWStWz8130_provenance
a
np:Provenance
.
dgn-np:NP247076.RAAowuyaCVCcrbtHd9_M0CJ2s2oH7SZpcoaX_jdWStWz8130_publicationInfo
a
np:PublicationInfo
.
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dgn-np:NP247076.RAAowuyaCVCcrbtHd9_M0CJ2s2oH7SZpcoaX_jdWStWz8130_assertion
{
miriam-gene:7515
a
ncit:C16612
.
lld:C0005695
a
ncit:C7057
.
dgn-gda:DGN7ce12df03ee586d0d528ed47efbe94ce
sio:SIO_000628
miriam-gene:7515
,
lld:C0005695
;
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.
}
dgn-np:NP247076.RAAowuyaCVCcrbtHd9_M0CJ2s2oH7SZpcoaX_jdWStWz8130_provenance
{
dgn-np:NP247076.RAAowuyaCVCcrbtHd9_M0CJ2s2oH7SZpcoaX_jdWStWz8130_assertion
dcterms:description
"[To evaluate whether these gene polymorphisms may be associated with an increased risk for bladder cancer or in association with p53 mutation status in bladder tumors, we screened for polymorphisms at XPD codons 751 and XRCC1 codon 399 in DNA isolated from blood of 194 bladder cancer patients and 313 healthy controls and for mutations in exons 4 to 8 of the p53 gene in bladder tumor DNA from 174 bladder cancer patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
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sio:SIO_000772
miriam-pubmed:20514470
;
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:NP247076.RAAowuyaCVCcrbtHd9_M0CJ2s2oH7SZpcoaX_jdWStWz8130_publicationInfo
{
this:
dcterms:created
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xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
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prv:usedData
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> , <
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> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
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pav:version
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}