@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP74150.RA-PMcIg23YtfGMknbKk16VCxxJIMLQDLrjf1fV15pbnI
> .
@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:NP74150.RA-PMcIg23YtfGMknbKk16VCxxJIMLQDLrjf1fV15pbnI130_head
{
this:
np:hasAssertion
dgn-np:NP74150.RA-PMcIg23YtfGMknbKk16VCxxJIMLQDLrjf1fV15pbnI130_assertion
;
np:hasProvenance
dgn-np:NP74150.RA-PMcIg23YtfGMknbKk16VCxxJIMLQDLrjf1fV15pbnI130_provenance
;
np:hasPublicationInfo
dgn-np:NP74150.RA-PMcIg23YtfGMknbKk16VCxxJIMLQDLrjf1fV15pbnI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP74150.RA-PMcIg23YtfGMknbKk16VCxxJIMLQDLrjf1fV15pbnI130_assertion
a
np:Assertion
.
dgn-np:NP74150.RA-PMcIg23YtfGMknbKk16VCxxJIMLQDLrjf1fV15pbnI130_provenance
a
np:Provenance
.
dgn-np:NP74150.RA-PMcIg23YtfGMknbKk16VCxxJIMLQDLrjf1fV15pbnI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP74150.RA-PMcIg23YtfGMknbKk16VCxxJIMLQDLrjf1fV15pbnI130_assertion
{
miriam-gene:2944
a
ncit:C16612
.
lld:C1956346
a
ncit:C7057
.
dgn-gda:DGN811acfd20914115c60937ddb40f82865
sio:SIO_000628
miriam-gene:2944
,
lld:C1956346
;
a
sio:SIO_001122
.
}
dgn-np:NP74150.RA-PMcIg23YtfGMknbKk16VCxxJIMLQDLrjf1fV15pbnI130_provenance
{
dgn-np:NP74150.RA-PMcIg23YtfGMknbKk16VCxxJIMLQDLrjf1fV15pbnI130_assertion
dcterms:description
"[Recent studies suggest that the common variant in the GSTM1 and GSTT1 genes modifies the risk of coronary artery disease (CAD), however, it is unclear whether the risk of CAD modulated by variants in the GSTM1 and GSTT1 genes was associated with alterations of indices of oxidative stress and inflammation.]. 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:19823950
;
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:NP74150.RA-PMcIg23YtfGMknbKk16VCxxJIMLQDLrjf1fV15pbnI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:36+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" .
}