@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP62228.RAi8NjFj7x_Ljbdeh-Jmbtbt_vm20PcCmrj7TJ26ftXjw
> .
@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:NP62228.RAi8NjFj7x_Ljbdeh-Jmbtbt_vm20PcCmrj7TJ26ftXjw130_head
{
this:
np:hasAssertion
dgn-np:NP62228.RAi8NjFj7x_Ljbdeh-Jmbtbt_vm20PcCmrj7TJ26ftXjw130_assertion
;
np:hasProvenance
dgn-np:NP62228.RAi8NjFj7x_Ljbdeh-Jmbtbt_vm20PcCmrj7TJ26ftXjw130_provenance
;
np:hasPublicationInfo
dgn-np:NP62228.RAi8NjFj7x_Ljbdeh-Jmbtbt_vm20PcCmrj7TJ26ftXjw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP62228.RAi8NjFj7x_Ljbdeh-Jmbtbt_vm20PcCmrj7TJ26ftXjw130_assertion
a
np:Assertion
.
dgn-np:NP62228.RAi8NjFj7x_Ljbdeh-Jmbtbt_vm20PcCmrj7TJ26ftXjw130_provenance
a
np:Provenance
.
dgn-np:NP62228.RAi8NjFj7x_Ljbdeh-Jmbtbt_vm20PcCmrj7TJ26ftXjw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP62228.RAi8NjFj7x_Ljbdeh-Jmbtbt_vm20PcCmrj7TJ26ftXjw130_assertion
{
miriam-gene:54600
a
ncit:C16612
.
lld:C0345904
a
ncit:C7057
.
dgn-gda:DGN2d84d09ed73de36499d3b4bb032024ba
sio:SIO_000628
miriam-gene:54600
,
lld:C0345904
;
a
sio:SIO_001122
.
}
dgn-np:NP62228.RAi8NjFj7x_Ljbdeh-Jmbtbt_vm20PcCmrj7TJ26ftXjw130_provenance
{
dgn-np:NP62228.RAi8NjFj7x_Ljbdeh-Jmbtbt_vm20PcCmrj7TJ26ftXjw130_assertion
dcterms:description
"[In conclusion, the mutant allele with one base insertion in the promoter region of the UGT1A9 gene would alter the level of enzyme expression and the metabolism of those drugs that are substrates of UGT1A9.]. 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:15115919
;
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:NP62228.RAi8NjFj7x_Ljbdeh-Jmbtbt_vm20PcCmrj7TJ26ftXjw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:29+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" .
}