@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1142911.RALU-CL9SGb-mFq5FX2zvIszG8bHiNoLcSmovgFCOCkHw
> .
@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/v4.0.0/void/
> .
dgn-np:NP1142911.RALU-CL9SGb-mFq5FX2zvIszG8bHiNoLcSmovgFCOCkHw130_head
{
this:
np:hasAssertion
dgn-np:NP1142911.RALU-CL9SGb-mFq5FX2zvIszG8bHiNoLcSmovgFCOCkHw130_assertion
;
np:hasProvenance
dgn-np:NP1142911.RALU-CL9SGb-mFq5FX2zvIszG8bHiNoLcSmovgFCOCkHw130_provenance
;
np:hasPublicationInfo
dgn-np:NP1142911.RALU-CL9SGb-mFq5FX2zvIszG8bHiNoLcSmovgFCOCkHw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1142911.RALU-CL9SGb-mFq5FX2zvIszG8bHiNoLcSmovgFCOCkHw130_assertion
a
np:Assertion
.
dgn-np:NP1142911.RALU-CL9SGb-mFq5FX2zvIszG8bHiNoLcSmovgFCOCkHw130_provenance
a
np:Provenance
.
dgn-np:NP1142911.RALU-CL9SGb-mFq5FX2zvIszG8bHiNoLcSmovgFCOCkHw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1142911.RALU-CL9SGb-mFq5FX2zvIszG8bHiNoLcSmovgFCOCkHw130_assertion
{
miriam-gene:133482
a
ncit:C16612
.
lld:C2239176
a
ncit:C7057
.
dgn-gda:DGNe5d2e3f73858aea6ed7b0fdb608cbd27
sio:SIO_000628
miriam-gene:133482
,
lld:C2239176
;
a
sio:SIO_001121
.
}
dgn-np:NP1142911.RALU-CL9SGb-mFq5FX2zvIszG8bHiNoLcSmovgFCOCkHw130_provenance
{
dgn-np:NP1142911.RALU-CL9SGb-mFq5FX2zvIszG8bHiNoLcSmovgFCOCkHw130_assertion
dcterms:description
"[The present meta-analysis demonstrated that the GSTM1 and GSTT1 null genotype may be associated with an increased risk of HCC and that individuals having the combination of both defective GST genotypes may be more susceptible to developing HCC.]. 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:24399650
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1142911.RALU-CL9SGb-mFq5FX2zvIszG8bHiNoLcSmovgFCOCkHw130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:50:24+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}