@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP412640.RARaDaKqreyhOjIqOuntsCgf7ODm6XiEGXP8EKDe89q4A
> .
@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:NP412640.RARaDaKqreyhOjIqOuntsCgf7ODm6XiEGXP8EKDe89q4A130_head
{
this:
np:hasAssertion
dgn-np:NP412640.RARaDaKqreyhOjIqOuntsCgf7ODm6XiEGXP8EKDe89q4A130_assertion
;
np:hasProvenance
dgn-np:NP412640.RARaDaKqreyhOjIqOuntsCgf7ODm6XiEGXP8EKDe89q4A130_provenance
;
np:hasPublicationInfo
dgn-np:NP412640.RARaDaKqreyhOjIqOuntsCgf7ODm6XiEGXP8EKDe89q4A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP412640.RARaDaKqreyhOjIqOuntsCgf7ODm6XiEGXP8EKDe89q4A130_assertion
a
np:Assertion
.
dgn-np:NP412640.RARaDaKqreyhOjIqOuntsCgf7ODm6XiEGXP8EKDe89q4A130_provenance
a
np:Provenance
.
dgn-np:NP412640.RARaDaKqreyhOjIqOuntsCgf7ODm6XiEGXP8EKDe89q4A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP412640.RARaDaKqreyhOjIqOuntsCgf7ODm6XiEGXP8EKDe89q4A130_assertion
{
miriam-gene:54658
a
ncit:C16612
.
lld:C0002871
a
ncit:C7057
.
dgn-gda:DGN59ffffdd67d05a373021421747b31ab8
sio:SIO_000628
miriam-gene:54658
,
lld:C0002871
;
a
sio:SIO_001121
.
}
dgn-np:NP412640.RARaDaKqreyhOjIqOuntsCgf7ODm6XiEGXP8EKDe89q4A130_provenance
{
dgn-np:NP412640.RARaDaKqreyhOjIqOuntsCgf7ODm6XiEGXP8EKDe89q4A130_assertion
dcterms:description
"[Our results illustrate the need for investigation of the effect of UGT1A variants other than (TA)(n) on the risk of irinotecan toxicity, as well as hyperbilirubinaemia due to hemolytic anaemia or human immunodeficiency virus protease inhibitors, so that appropriate pharmacogenetic advice can be given.]. 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:21309756
;
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:NP412640.RARaDaKqreyhOjIqOuntsCgf7ODm6XiEGXP8EKDe89q4A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:05+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" .
}