@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP59106.RAgGJTBJX8Rw6OBPe0kuwLQPxkYmK0Qq55bO6jyDy7VGA
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP59106.RAgGJTBJX8Rw6OBPe0kuwLQPxkYmK0Qq55bO6jyDy7VGA130_assertion
;
np:hasProvenance
dgn-np:NP59106.RAgGJTBJX8Rw6OBPe0kuwLQPxkYmK0Qq55bO6jyDy7VGA130_provenance
;
np:hasPublicationInfo
dgn-np:NP59106.RAgGJTBJX8Rw6OBPe0kuwLQPxkYmK0Qq55bO6jyDy7VGA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP59106.RAgGJTBJX8Rw6OBPe0kuwLQPxkYmK0Qq55bO6jyDy7VGA130_assertion
a
np:Assertion
.
dgn-np:NP59106.RAgGJTBJX8Rw6OBPe0kuwLQPxkYmK0Qq55bO6jyDy7VGA130_provenance
a
np:Provenance
.
dgn-np:NP59106.RAgGJTBJX8Rw6OBPe0kuwLQPxkYmK0Qq55bO6jyDy7VGA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP59106.RAgGJTBJX8Rw6OBPe0kuwLQPxkYmK0Qq55bO6jyDy7VGA130_assertion
{
miriam-gene:7421
a
ncit:C16612
.
lld:C0023418
a
ncit:C7057
.
dgn-gda:DGN3fd9f2dea46e68e66a559b67a4e3454d
sio:SIO_000628
miriam-gene:7421
,
lld:C0023418
;
a
sio:SIO_001122
.
}
dgn-np:NP59106.RAgGJTBJX8Rw6OBPe0kuwLQPxkYmK0Qq55bO6jyDy7VGA130_provenance
{
dgn-np:NP59106.RAgGJTBJX8Rw6OBPe0kuwLQPxkYmK0Qq55bO6jyDy7VGA130_assertion
dcterms:description
"[The UGT1A1 6/6 genotype predicted lower catechol AUC. Prednisone strongly induces etoposide clearance, genetic polymorphisms may predict the constitutive and induced clearance of etoposide, and the relationship between genotype and phenotype differs by race.]. 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:12969965
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP59106.RAgGJTBJX8Rw6OBPe0kuwLQPxkYmK0Qq55bO6jyDy7VGA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:27+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
<
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> , <
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" .
}