@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP55154.RAsDg1bIaMk5z5Plf-0gz0dCDNjtlGwOAHH_ouls7GIj4
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP55154.RAsDg1bIaMk5z5Plf-0gz0dCDNjtlGwOAHH_ouls7GIj4130_head
{
this:
np:hasAssertion
dgn-np:NP55154.RAsDg1bIaMk5z5Plf-0gz0dCDNjtlGwOAHH_ouls7GIj4130_assertion
;
np:hasProvenance
dgn-np:NP55154.RAsDg1bIaMk5z5Plf-0gz0dCDNjtlGwOAHH_ouls7GIj4130_provenance
;
np:hasPublicationInfo
dgn-np:NP55154.RAsDg1bIaMk5z5Plf-0gz0dCDNjtlGwOAHH_ouls7GIj4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP55154.RAsDg1bIaMk5z5Plf-0gz0dCDNjtlGwOAHH_ouls7GIj4130_assertion
a
np:Assertion
.
dgn-np:NP55154.RAsDg1bIaMk5z5Plf-0gz0dCDNjtlGwOAHH_ouls7GIj4130_provenance
a
np:Provenance
.
dgn-np:NP55154.RAsDg1bIaMk5z5Plf-0gz0dCDNjtlGwOAHH_ouls7GIj4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP55154.RAsDg1bIaMk5z5Plf-0gz0dCDNjtlGwOAHH_ouls7GIj4130_assertion
{
miriam-gene:1548
a
ncit:C16612
.
lld:C0024623
a
ncit:C7057
.
dgn-gda:DGN5fc6fceb5bbe0f814b7bf61efb4b8e66
sio:SIO_000628
miriam-gene:1548
,
lld:C0024623
;
a
sio:SIO_001122
.
}
dgn-np:NP55154.RAsDg1bIaMk5z5Plf-0gz0dCDNjtlGwOAHH_ouls7GIj4130_provenance
{
dgn-np:NP55154.RAsDg1bIaMk5z5Plf-0gz0dCDNjtlGwOAHH_ouls7GIj4130_assertion
dcterms:description
"[The frequency with which the subjects carried homozygotes of the CYP2A6 gene deletion allele, which causes lack of the enzyme activity, was significantly higher in the gastric cancer patients than in the healthy control subjects (OR = 3.14, 95% confidence interval (95% CI) = 1.05-9.41).]. 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:12115524
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP55154.RAsDg1bIaMk5z5Plf-0gz0dCDNjtlGwOAHH_ouls7GIj4130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:10+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}