@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP70901.RAZiYD2WRNfW7neJh5WO7KGYj8_MpLcS-KtcupBDsQ4Jg
> .
@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:NP70901.RAZiYD2WRNfW7neJh5WO7KGYj8_MpLcS-KtcupBDsQ4Jg130_head
{
this:
np:hasAssertion
dgn-np:NP70901.RAZiYD2WRNfW7neJh5WO7KGYj8_MpLcS-KtcupBDsQ4Jg130_assertion
;
np:hasProvenance
dgn-np:NP70901.RAZiYD2WRNfW7neJh5WO7KGYj8_MpLcS-KtcupBDsQ4Jg130_provenance
;
np:hasPublicationInfo
dgn-np:NP70901.RAZiYD2WRNfW7neJh5WO7KGYj8_MpLcS-KtcupBDsQ4Jg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP70901.RAZiYD2WRNfW7neJh5WO7KGYj8_MpLcS-KtcupBDsQ4Jg130_assertion
a
np:Assertion
.
dgn-np:NP70901.RAZiYD2WRNfW7neJh5WO7KGYj8_MpLcS-KtcupBDsQ4Jg130_provenance
a
np:Provenance
.
dgn-np:NP70901.RAZiYD2WRNfW7neJh5WO7KGYj8_MpLcS-KtcupBDsQ4Jg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP70901.RAZiYD2WRNfW7neJh5WO7KGYj8_MpLcS-KtcupBDsQ4Jg130_assertion
{
miriam-gene:4536
a
ncit:C16612
.
lld:C1527249
a
ncit:C7057
.
dgn-gda:DGN16f0f9039c49d944c964c4b39b2bf080
sio:SIO_000628
miriam-gene:4536
,
lld:C1527249
;
a
sio:SIO_001122
.
}
dgn-np:NP70901.RAZiYD2WRNfW7neJh5WO7KGYj8_MpLcS-KtcupBDsQ4Jg130_provenance
{
dgn-np:NP70901.RAZiYD2WRNfW7neJh5WO7KGYj8_MpLcS-KtcupBDsQ4Jg130_assertion
dct:description
"[After applying three Cox proportional hazard models adjusted for American Joint Committee on Cancer (AJCC) stage, age and sex, three single nucleotide polymorphisms, two located in the 12S ribosomal RNA region (G752A and G1440A) and one in the nicotinamide adenine dinucleotide dehydrogenase subunit 2 region (ND2) region (G4770A), were statistically significantly associated with all-cause (Model I P-values: 0.0001, 0.002 and 0.002, respectively) and CRC-specific mortality (Model I P-values: 5 x 10(-5), 0.0003 and 0.0006, respectively).]. 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:19945968
;
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:NP70901.RAZiYD2WRNfW7neJh5WO7KGYj8_MpLcS-KtcupBDsQ4Jg130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:34+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" .
}