@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP772252.RAvrKQmBGrIxRsX1xFqCu_gwZZ-CXhPD322zk9w6773cQ
> .
@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:NP772252.RAvrKQmBGrIxRsX1xFqCu_gwZZ-CXhPD322zk9w6773cQ130_head
{
this:
np:hasAssertion
dgn-np:NP772252.RAvrKQmBGrIxRsX1xFqCu_gwZZ-CXhPD322zk9w6773cQ130_assertion
;
np:hasProvenance
dgn-np:NP772252.RAvrKQmBGrIxRsX1xFqCu_gwZZ-CXhPD322zk9w6773cQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP772252.RAvrKQmBGrIxRsX1xFqCu_gwZZ-CXhPD322zk9w6773cQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP772252.RAvrKQmBGrIxRsX1xFqCu_gwZZ-CXhPD322zk9w6773cQ130_assertion
a
np:Assertion
.
dgn-np:NP772252.RAvrKQmBGrIxRsX1xFqCu_gwZZ-CXhPD322zk9w6773cQ130_provenance
a
np:Provenance
.
dgn-np:NP772252.RAvrKQmBGrIxRsX1xFqCu_gwZZ-CXhPD322zk9w6773cQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP772252.RAvrKQmBGrIxRsX1xFqCu_gwZZ-CXhPD322zk9w6773cQ130_assertion
{
miriam-gene:4899
a
ncit:C16612
.
lld:C0011991
a
ncit:C7057
.
dgn-gda:DGN4c7641331928b247c9d8b501f7953c2e
sio:SIO_000628
miriam-gene:4899
,
lld:C0011991
;
a
sio:SIO_001121
.
}
dgn-np:NP772252.RAvrKQmBGrIxRsX1xFqCu_gwZZ-CXhPD322zk9w6773cQ130_provenance
{
dgn-np:NP772252.RAvrKQmBGrIxRsX1xFqCu_gwZZ-CXhPD322zk9w6773cQ130_assertion
dcterms:description
"[The EGAPP Working Group (EWG) found no intervention trials showing that targeted dosing of irinotecan based on UGT1A1 genotyping could reduce the rates of two specific adverse drug events, severe (Grade 3-4) neutropenia or diarrhea.]. 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:19125128
;
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:NP772252.RAvrKQmBGrIxRsX1xFqCu_gwZZ-CXhPD322zk9w6773cQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:47+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" .
}