@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP167176.RATKMwaUUX8KCc32dJu_81hCAxDyQA_vSkaM-wqFF4urI
> .
@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:NP167176.RATKMwaUUX8KCc32dJu_81hCAxDyQA_vSkaM-wqFF4urI130_head
{
this:
np:hasAssertion
dgn-np:NP167176.RATKMwaUUX8KCc32dJu_81hCAxDyQA_vSkaM-wqFF4urI130_assertion
;
np:hasProvenance
dgn-np:NP167176.RATKMwaUUX8KCc32dJu_81hCAxDyQA_vSkaM-wqFF4urI130_provenance
;
np:hasPublicationInfo
dgn-np:NP167176.RATKMwaUUX8KCc32dJu_81hCAxDyQA_vSkaM-wqFF4urI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP167176.RATKMwaUUX8KCc32dJu_81hCAxDyQA_vSkaM-wqFF4urI130_assertion
a
np:Assertion
.
dgn-np:NP167176.RATKMwaUUX8KCc32dJu_81hCAxDyQA_vSkaM-wqFF4urI130_provenance
a
np:Provenance
.
dgn-np:NP167176.RATKMwaUUX8KCc32dJu_81hCAxDyQA_vSkaM-wqFF4urI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP167176.RATKMwaUUX8KCc32dJu_81hCAxDyQA_vSkaM-wqFF4urI130_assertion
{
miriam-gene:7298
a
ncit:C16612
.
lld:C0021843
a
ncit:C7057
.
dgn-gda:DGN49fe38e6be5e745b943e2d396c5c110d
sio:SIO_000628
miriam-gene:7298
,
lld:C0021843
;
a
sio:SIO_001121
.
}
dgn-np:NP167176.RATKMwaUUX8KCc32dJu_81hCAxDyQA_vSkaM-wqFF4urI130_provenance
{
dgn-np:NP167176.RATKMwaUUX8KCc32dJu_81hCAxDyQA_vSkaM-wqFF4urI130_assertion
dcterms:description
"[Cox multivariate analysis, adjusted for the prognostic impact of disease stage, vascular tumor invasion, and bowel obstruction at resection, revealed that high TYMS gene copy number was associated with significantly higher risk of recurrence (HR = 1.6; 95%CI 1.1-2.2; p = 0.02) and death (HR = 1.6; 95%CI 1.1-2.3; p = 0.01).]. 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:18607850
;
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:NP167176.RATKMwaUUX8KCc32dJu_81hCAxDyQA_vSkaM-wqFF4urI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:30+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" .
}