@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP56565.RA4eSjg0b2kV9bLquIZXRLMPrO4rRBZNDKzX5TvqrClIk
> .
@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 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:NP56565.RA4eSjg0b2kV9bLquIZXRLMPrO4rRBZNDKzX5TvqrClIk130_head
{
this:
np:hasAssertion
dgn-np:NP56565.RA4eSjg0b2kV9bLquIZXRLMPrO4rRBZNDKzX5TvqrClIk130_assertion
;
np:hasProvenance
dgn-np:NP56565.RA4eSjg0b2kV9bLquIZXRLMPrO4rRBZNDKzX5TvqrClIk130_provenance
;
np:hasPublicationInfo
dgn-np:NP56565.RA4eSjg0b2kV9bLquIZXRLMPrO4rRBZNDKzX5TvqrClIk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP56565.RA4eSjg0b2kV9bLquIZXRLMPrO4rRBZNDKzX5TvqrClIk130_assertion
a
np:Assertion
.
dgn-np:NP56565.RA4eSjg0b2kV9bLquIZXRLMPrO4rRBZNDKzX5TvqrClIk130_provenance
a
np:Provenance
.
dgn-np:NP56565.RA4eSjg0b2kV9bLquIZXRLMPrO4rRBZNDKzX5TvqrClIk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP56565.RA4eSjg0b2kV9bLquIZXRLMPrO4rRBZNDKzX5TvqrClIk130_assertion
{
miriam-gene:3606
a
ncit:C16612
.
lld:C0238301
a
ncit:C7057
.
dgn-gda:DGN654b745407652c8b2480f14a76861713
sio:SIO_000628
miriam-gene:3606
,
lld:C0238301
;
a
sio:SIO_001122
.
}
dgn-np:NP56565.RA4eSjg0b2kV9bLquIZXRLMPrO4rRBZNDKzX5TvqrClIk130_provenance
{
dgn-np:NP56565.RA4eSjg0b2kV9bLquIZXRLMPrO4rRBZNDKzX5TvqrClIk130_assertion
dct:description
"[ This study was performed to improve the definition of the pathogenetic factors implicated in UCNT by addressing the correlation between cytokine polymorphisms and clinical parameters. This is the first study investigating the possible role of the IL-18 and IL-10 polymorphisms in the development and outcome of UCNT. In our genetic analysis there is no evidence for involvement of IL-10 promoter polymorphisms alone in the genetic predisposition to this tumor. On the other hand, IL18 genetic variants may represent a genetic risk factor for tumor aggressiveness.]. 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:16059673
;
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:NP56565.RA4eSjg0b2kV9bLquIZXRLMPrO4rRBZNDKzX5TvqrClIk130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:26+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}