@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP497410.RAknSV0M28r31yqdQRvEfIIiHfpvF6I7J6C_hQPd6WZZ8
> .
@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:NP497410.RAknSV0M28r31yqdQRvEfIIiHfpvF6I7J6C_hQPd6WZZ8130_head
{
this:
np:hasAssertion
dgn-np:NP497410.RAknSV0M28r31yqdQRvEfIIiHfpvF6I7J6C_hQPd6WZZ8130_assertion
;
np:hasProvenance
dgn-np:NP497410.RAknSV0M28r31yqdQRvEfIIiHfpvF6I7J6C_hQPd6WZZ8130_provenance
;
np:hasPublicationInfo
dgn-np:NP497410.RAknSV0M28r31yqdQRvEfIIiHfpvF6I7J6C_hQPd6WZZ8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP497410.RAknSV0M28r31yqdQRvEfIIiHfpvF6I7J6C_hQPd6WZZ8130_assertion
a
np:Assertion
.
dgn-np:NP497410.RAknSV0M28r31yqdQRvEfIIiHfpvF6I7J6C_hQPd6WZZ8130_provenance
a
np:Provenance
.
dgn-np:NP497410.RAknSV0M28r31yqdQRvEfIIiHfpvF6I7J6C_hQPd6WZZ8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP497410.RAknSV0M28r31yqdQRvEfIIiHfpvF6I7J6C_hQPd6WZZ8130_assertion
{
miriam-gene:51151
a
ncit:C16612
.
lld:C0017551
a
ncit:C7057
.
dgn-gda:DGN006eab02ae9bcb9f23615fead731690e
sio:SIO_000628
miriam-gene:51151
,
lld:C0017551
;
a
sio:SIO_001121
.
}
dgn-np:NP497410.RAknSV0M28r31yqdQRvEfIIiHfpvF6I7J6C_hQPd6WZZ8130_provenance
{
dgn-np:NP497410.RAknSV0M28r31yqdQRvEfIIiHfpvF6I7J6C_hQPd6WZZ8130_assertion
dcterms:description
"[We wanted to assess polymorphisms in the uridine diphosphoglucuronosyl transferase 1A1 (UGT 1A1) gene: the TATA box polymorphism and UGT 1A1 G71R and Y486D mutations in the coding sequence, the main mutations characterizing Gilbert's syndrome, as predictors of severe toxic event occurrence after irinotecan (CPT-11) administration.]. 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:15297419
;
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:NP497410.RAknSV0M28r31yqdQRvEfIIiHfpvF6I7J6C_hQPd6WZZ8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:56+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" .
}