@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP374312.RAldqG6zyOBtZ_2xNCekzRZH_fYusfz-ruyyO7erlfOmM
> .
@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:NP374312.RAldqG6zyOBtZ_2xNCekzRZH_fYusfz-ruyyO7erlfOmM130_head
{
this:
np:hasAssertion
dgn-np:NP374312.RAldqG6zyOBtZ_2xNCekzRZH_fYusfz-ruyyO7erlfOmM130_assertion
;
np:hasProvenance
dgn-np:NP374312.RAldqG6zyOBtZ_2xNCekzRZH_fYusfz-ruyyO7erlfOmM130_provenance
;
np:hasPublicationInfo
dgn-np:NP374312.RAldqG6zyOBtZ_2xNCekzRZH_fYusfz-ruyyO7erlfOmM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP374312.RAldqG6zyOBtZ_2xNCekzRZH_fYusfz-ruyyO7erlfOmM130_assertion
a
np:Assertion
.
dgn-np:NP374312.RAldqG6zyOBtZ_2xNCekzRZH_fYusfz-ruyyO7erlfOmM130_provenance
a
np:Provenance
.
dgn-np:NP374312.RAldqG6zyOBtZ_2xNCekzRZH_fYusfz-ruyyO7erlfOmM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP374312.RAldqG6zyOBtZ_2xNCekzRZH_fYusfz-ruyyO7erlfOmM130_assertion
{
miriam-gene:1559
a
ncit:C16612
.
lld:C0014544
a
ncit:C7057
.
dgn-gda:DGN9c9d78bd9580744b6440a28a31756700
sio:SIO_000628
miriam-gene:1559
,
lld:C0014544
;
a
sio:SIO_001121
.
}
dgn-np:NP374312.RAldqG6zyOBtZ_2xNCekzRZH_fYusfz-ruyyO7erlfOmM130_provenance
{
dgn-np:NP374312.RAldqG6zyOBtZ_2xNCekzRZH_fYusfz-ruyyO7erlfOmM130_assertion
dcterms:description
"[The aim of this study was to determine the relationship between plasma concentrations of VPA and single nucleotide polymorphisms (SNPs) involving uridine diphosphate glucuronosyltransferase (UGT) 1A6 (UGT1A6), UGT2B7, and cytochrome P450 2C9 (CYP2C9) genes in Chinese children with epilepsy.]. 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:23099353
;
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:NP374312.RAldqG6zyOBtZ_2xNCekzRZH_fYusfz-ruyyO7erlfOmM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:39+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" .
}