@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP295015.RAh795W4rGs8dEpX3twE1Jch5FJhYdqcsbeGiAy4RNkYI
> .
@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:NP295015.RAh795W4rGs8dEpX3twE1Jch5FJhYdqcsbeGiAy4RNkYI130_head
{
this:
np:hasAssertion
dgn-np:NP295015.RAh795W4rGs8dEpX3twE1Jch5FJhYdqcsbeGiAy4RNkYI130_assertion
;
np:hasProvenance
dgn-np:NP295015.RAh795W4rGs8dEpX3twE1Jch5FJhYdqcsbeGiAy4RNkYI130_provenance
;
np:hasPublicationInfo
dgn-np:NP295015.RAh795W4rGs8dEpX3twE1Jch5FJhYdqcsbeGiAy4RNkYI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP295015.RAh795W4rGs8dEpX3twE1Jch5FJhYdqcsbeGiAy4RNkYI130_assertion
a
np:Assertion
.
dgn-np:NP295015.RAh795W4rGs8dEpX3twE1Jch5FJhYdqcsbeGiAy4RNkYI130_provenance
a
np:Provenance
.
dgn-np:NP295015.RAh795W4rGs8dEpX3twE1Jch5FJhYdqcsbeGiAy4RNkYI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP295015.RAh795W4rGs8dEpX3twE1Jch5FJhYdqcsbeGiAy4RNkYI130_assertion
{
miriam-gene:133482
a
ncit:C16612
.
lld:C0085669
a
ncit:C7057
.
dgn-gda:DGN5e167347b57c27eb35945e698cd1ddb6
sio:SIO_000628
miriam-gene:133482
,
lld:C0085669
;
a
sio:SIO_001121
.
}
dgn-np:NP295015.RAh795W4rGs8dEpX3twE1Jch5FJhYdqcsbeGiAy4RNkYI130_provenance
{
dgn-np:NP295015.RAh795W4rGs8dEpX3twE1Jch5FJhYdqcsbeGiAy4RNkYI130_assertion
dcterms:description
"[Hence GST genotyping can be made mandatory in management of acute leukemia so that more aggressive therapy such as allogenic stem cell transplantation may be planned in the case of patients with a null genotype.]. 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-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
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:NP295015.RAh795W4rGs8dEpX3twE1Jch5FJhYdqcsbeGiAy4RNkYI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:47+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" .
}