@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP90973.RANsIAY7fCnZBR5uXv2BhZvlr_3vPFNc64QNGr10TmNs8
> .
@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:NP90973.RANsIAY7fCnZBR5uXv2BhZvlr_3vPFNc64QNGr10TmNs8130_head
{
this:
np:hasAssertion
dgn-np:NP90973.RANsIAY7fCnZBR5uXv2BhZvlr_3vPFNc64QNGr10TmNs8130_assertion
;
np:hasProvenance
dgn-np:NP90973.RANsIAY7fCnZBR5uXv2BhZvlr_3vPFNc64QNGr10TmNs8130_provenance
;
np:hasPublicationInfo
dgn-np:NP90973.RANsIAY7fCnZBR5uXv2BhZvlr_3vPFNc64QNGr10TmNs8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP90973.RANsIAY7fCnZBR5uXv2BhZvlr_3vPFNc64QNGr10TmNs8130_assertion
a
np:Assertion
.
dgn-np:NP90973.RANsIAY7fCnZBR5uXv2BhZvlr_3vPFNc64QNGr10TmNs8130_provenance
a
np:Provenance
.
dgn-np:NP90973.RANsIAY7fCnZBR5uXv2BhZvlr_3vPFNc64QNGr10TmNs8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP90973.RANsIAY7fCnZBR5uXv2BhZvlr_3vPFNc64QNGr10TmNs8130_assertion
{
miriam-gene:2944
a
ncit:C16612
.
lld:C0023418
a
ncit:C7057
.
dgn-gda:DGN12ca65df2788102e499f820e1f8d333a
sio:SIO_000628
miriam-gene:2944
,
lld:C0023418
;
a
sio:SIO_001122
.
}
dgn-np:NP90973.RANsIAY7fCnZBR5uXv2BhZvlr_3vPFNc64QNGr10TmNs8130_provenance
{
dgn-np:NP90973.RANsIAY7fCnZBR5uXv2BhZvlr_3vPFNc64QNGr10TmNs8130_assertion
dcterms:description
"[ transition in exon 5 of GSTP1 gene (alone or combined with GSTM1 deletion) may be one of the molecular predictors of higher susceptibility to acute leukaemia in children. but not of the clinical course of this disease.]. 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:15738600
;
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:NP90973.RANsIAY7fCnZBR5uXv2BhZvlr_3vPFNc64QNGr10TmNs8130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:42:29+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" .
}