@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1082311.RAHiumVMNGzL6VnEnR5SHOSRgaGrJXVFcSP4KGB20f_Us
> .
@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:NP1082311.RAHiumVMNGzL6VnEnR5SHOSRgaGrJXVFcSP4KGB20f_Us130_head
{
this:
np:hasAssertion
dgn-np:NP1082311.RAHiumVMNGzL6VnEnR5SHOSRgaGrJXVFcSP4KGB20f_Us130_assertion
;
np:hasProvenance
dgn-np:NP1082311.RAHiumVMNGzL6VnEnR5SHOSRgaGrJXVFcSP4KGB20f_Us130_provenance
;
np:hasPublicationInfo
dgn-np:NP1082311.RAHiumVMNGzL6VnEnR5SHOSRgaGrJXVFcSP4KGB20f_Us130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1082311.RAHiumVMNGzL6VnEnR5SHOSRgaGrJXVFcSP4KGB20f_Us130_assertion
a
np:Assertion
.
dgn-np:NP1082311.RAHiumVMNGzL6VnEnR5SHOSRgaGrJXVFcSP4KGB20f_Us130_provenance
a
np:Provenance
.
dgn-np:NP1082311.RAHiumVMNGzL6VnEnR5SHOSRgaGrJXVFcSP4KGB20f_Us130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1082311.RAHiumVMNGzL6VnEnR5SHOSRgaGrJXVFcSP4KGB20f_Us130_assertion
{
miriam-gene:2952
a
ncit:C16612
.
lld:C0023467
a
ncit:C7057
.
dgn-gda:DGN690250d74a51d57b595c20bb2d1ce518
sio:SIO_000628
miriam-gene:2952
,
lld:C0023467
;
a
sio:SIO_001121
.
}
dgn-np:NP1082311.RAHiumVMNGzL6VnEnR5SHOSRgaGrJXVFcSP4KGB20f_Us130_provenance
{
dgn-np:NP1082311.RAHiumVMNGzL6VnEnR5SHOSRgaGrJXVFcSP4KGB20f_Us130_assertion
dcterms:description
"[Significantly increased frequencies of GSTM1 null genotype (M0), GSTT1 null genotype (T0) and GST double null genotype (T0M0) were observed in the both ALL and AML cases as compared to controls.]. 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:23725116
;
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:NP1082311.RAHiumVMNGzL6VnEnR5SHOSRgaGrJXVFcSP4KGB20f_Us130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:56+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" .
}