@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP383609.RApr-HYKaNgzC9ccWsvOa0S-ubPqIgUurL9F9Zu755_kw
> .
@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:NP383609.RApr-HYKaNgzC9ccWsvOa0S-ubPqIgUurL9F9Zu755_kw130_head
{
this:
np:hasAssertion
dgn-np:NP383609.RApr-HYKaNgzC9ccWsvOa0S-ubPqIgUurL9F9Zu755_kw130_assertion
;
np:hasProvenance
dgn-np:NP383609.RApr-HYKaNgzC9ccWsvOa0S-ubPqIgUurL9F9Zu755_kw130_provenance
;
np:hasPublicationInfo
dgn-np:NP383609.RApr-HYKaNgzC9ccWsvOa0S-ubPqIgUurL9F9Zu755_kw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP383609.RApr-HYKaNgzC9ccWsvOa0S-ubPqIgUurL9F9Zu755_kw130_assertion
a
np:Assertion
.
dgn-np:NP383609.RApr-HYKaNgzC9ccWsvOa0S-ubPqIgUurL9F9Zu755_kw130_provenance
a
np:Provenance
.
dgn-np:NP383609.RApr-HYKaNgzC9ccWsvOa0S-ubPqIgUurL9F9Zu755_kw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP383609.RApr-HYKaNgzC9ccWsvOa0S-ubPqIgUurL9F9Zu755_kw130_assertion
{
miriam-gene:23158
a
ncit:C16612
.
lld:C0023452
a
ncit:C7057
.
dgn-gda:DGN745fa7a89aea3e2c942c857e4bc6b041
sio:SIO_000628
miriam-gene:23158
,
lld:C0023452
;
a
sio:SIO_001121
.
}
dgn-np:NP383609.RApr-HYKaNgzC9ccWsvOa0S-ubPqIgUurL9F9Zu755_kw130_provenance
{
dgn-np:NP383609.RApr-HYKaNgzC9ccWsvOa0S-ubPqIgUurL9F9Zu755_kw130_assertion
dcterms:description
"[In a matched case-control study, we investigated the associations between CNS relapse in childhood ALL and the presence of phenotypically relevant single nucleotide polymorphisms within the GSTP1 (codon 105 and 114) and MDR1 genes (ABCB1; coding for Pgp; exon 26, C3435T).]. 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:15717687
;
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:NP383609.RApr-HYKaNgzC9ccWsvOa0S-ubPqIgUurL9F9Zu755_kw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:48+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" .
}