@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP640343.RAYZkRXbLJN51udV7PEPdeGfEKMt_bqnAJu29-4cq-Lj8
> .
@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:NP640343.RAYZkRXbLJN51udV7PEPdeGfEKMt_bqnAJu29-4cq-Lj8130_head
{
this:
np:hasAssertion
dgn-np:NP640343.RAYZkRXbLJN51udV7PEPdeGfEKMt_bqnAJu29-4cq-Lj8130_assertion
;
np:hasProvenance
dgn-np:NP640343.RAYZkRXbLJN51udV7PEPdeGfEKMt_bqnAJu29-4cq-Lj8130_provenance
;
np:hasPublicationInfo
dgn-np:NP640343.RAYZkRXbLJN51udV7PEPdeGfEKMt_bqnAJu29-4cq-Lj8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP640343.RAYZkRXbLJN51udV7PEPdeGfEKMt_bqnAJu29-4cq-Lj8130_assertion
a
np:Assertion
.
dgn-np:NP640343.RAYZkRXbLJN51udV7PEPdeGfEKMt_bqnAJu29-4cq-Lj8130_provenance
a
np:Provenance
.
dgn-np:NP640343.RAYZkRXbLJN51udV7PEPdeGfEKMt_bqnAJu29-4cq-Lj8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP640343.RAYZkRXbLJN51udV7PEPdeGfEKMt_bqnAJu29-4cq-Lj8130_assertion
{
miriam-gene:2950
a
ncit:C16612
.
lld:C0854467
a
ncit:C7057
.
dgn-gda:DGN6cee41d368440fcb0b2c695db0124628
sio:SIO_000628
miriam-gene:2950
,
lld:C0854467
;
a
sio:SIO_001121
.
}
dgn-np:NP640343.RAYZkRXbLJN51udV7PEPdeGfEKMt_bqnAJu29-4cq-Lj8130_provenance
{
dgn-np:NP640343.RAYZkRXbLJN51udV7PEPdeGfEKMt_bqnAJu29-4cq-Lj8130_assertion
dcterms:description
"[In the present study, the effects of common GSTM1, GSTT1, and GSTP1 genetic mutations on the severity of myelosuppression, gastrointestinal (GI) toxicity, and infection incidences induced by pulsed CTX therapy were evaluated in patients SLE.]. 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:16995867
;
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:NP640343.RAYZkRXbLJN51udV7PEPdeGfEKMt_bqnAJu29-4cq-Lj8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:26+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" .
}