@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP74049.RAgdZ2X6csRhLgV82r4E1ZxFaMXWtKXmdtmR3oQfsJIEI
> .
@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:NP74049.RAgdZ2X6csRhLgV82r4E1ZxFaMXWtKXmdtmR3oQfsJIEI130_head
{
this:
np:hasAssertion
dgn-np:NP74049.RAgdZ2X6csRhLgV82r4E1ZxFaMXWtKXmdtmR3oQfsJIEI130_assertion
;
np:hasProvenance
dgn-np:NP74049.RAgdZ2X6csRhLgV82r4E1ZxFaMXWtKXmdtmR3oQfsJIEI130_provenance
;
np:hasPublicationInfo
dgn-np:NP74049.RAgdZ2X6csRhLgV82r4E1ZxFaMXWtKXmdtmR3oQfsJIEI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP74049.RAgdZ2X6csRhLgV82r4E1ZxFaMXWtKXmdtmR3oQfsJIEI130_assertion
a
np:Assertion
.
dgn-np:NP74049.RAgdZ2X6csRhLgV82r4E1ZxFaMXWtKXmdtmR3oQfsJIEI130_provenance
a
np:Provenance
.
dgn-np:NP74049.RAgdZ2X6csRhLgV82r4E1ZxFaMXWtKXmdtmR3oQfsJIEI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP74049.RAgdZ2X6csRhLgV82r4E1ZxFaMXWtKXmdtmR3oQfsJIEI130_assertion
{
miriam-gene:2947
a
ncit:C16612
.
lld:C1566590
a
ncit:C7057
.
dgn-gda:DGNb6c7c4cd1ec522928faa2854c764a134
sio:SIO_000628
miriam-gene:2947
,
lld:C1566590
;
a
sio:SIO_001122
.
}
dgn-np:NP74049.RAgdZ2X6csRhLgV82r4E1ZxFaMXWtKXmdtmR3oQfsJIEI130_provenance
{
dgn-np:NP74049.RAgdZ2X6csRhLgV82r4E1ZxFaMXWtKXmdtmR3oQfsJIEI130_assertion
dcterms:description
"[Patients with variant genotype of GSTM1 and GSTP1 were at higher risk for rejection and delayed functioning of the allograft, respectively, supporting the hypothesis for involvement of GST isoform variants in allograft outcome in renal transplant recipien]. 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:19486347
;
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:NP74049.RAgdZ2X6csRhLgV82r4E1ZxFaMXWtKXmdtmR3oQfsJIEI130_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" .
}