@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP384926.RANUrjNUvto_YlOixo8lYA4mUsA2uBfhKKRxqe4Ags4Ho
> .
@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:NP384926.RANUrjNUvto_YlOixo8lYA4mUsA2uBfhKKRxqe4Ags4Ho130_head
{
this:
np:hasAssertion
dgn-np:NP384926.RANUrjNUvto_YlOixo8lYA4mUsA2uBfhKKRxqe4Ags4Ho130_assertion
;
np:hasProvenance
dgn-np:NP384926.RANUrjNUvto_YlOixo8lYA4mUsA2uBfhKKRxqe4Ags4Ho130_provenance
;
np:hasPublicationInfo
dgn-np:NP384926.RANUrjNUvto_YlOixo8lYA4mUsA2uBfhKKRxqe4Ags4Ho130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP384926.RANUrjNUvto_YlOixo8lYA4mUsA2uBfhKKRxqe4Ags4Ho130_assertion
a
np:Assertion
.
dgn-np:NP384926.RANUrjNUvto_YlOixo8lYA4mUsA2uBfhKKRxqe4Ags4Ho130_provenance
a
np:Provenance
.
dgn-np:NP384926.RANUrjNUvto_YlOixo8lYA4mUsA2uBfhKKRxqe4Ags4Ho130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP384926.RANUrjNUvto_YlOixo8lYA4mUsA2uBfhKKRxqe4Ags4Ho130_assertion
{
miriam-gene:1728
a
ncit:C16612
.
lld:C0005684
a
ncit:C7057
.
dgn-gda:DGN3e02b65e72c08abe0219e45fe54d7fac
sio:SIO_000628
miriam-gene:1728
,
lld:C0005684
;
a
sio:SIO_001121
.
}
dgn-np:NP384926.RANUrjNUvto_YlOixo8lYA4mUsA2uBfhKKRxqe4Ags4Ho130_provenance
{
dgn-np:NP384926.RANUrjNUvto_YlOixo8lYA4mUsA2uBfhKKRxqe4Ags4Ho130_assertion
dcterms:description
"[We conducted a hospital based case-control study to evaluate the potential association between genetic polymorphisms of CYP2E1 (C1019T in the 5' flanking region) and NQO1 (C609T in exon 6) and bladder cancer risk in Asian population.]. 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:12777965
;
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:NP384926.RANUrjNUvto_YlOixo8lYA4mUsA2uBfhKKRxqe4Ags4Ho130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:49+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
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"v2.1.0" .
}