@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP311691.RAV0OgI3ejRSkT94CgXuVEzSmIKADNellQbDv9sp7K4yA
> .
@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:NP311691.RAV0OgI3ejRSkT94CgXuVEzSmIKADNellQbDv9sp7K4yA130_head
{
this:
np:hasAssertion
dgn-np:NP311691.RAV0OgI3ejRSkT94CgXuVEzSmIKADNellQbDv9sp7K4yA130_assertion
;
np:hasProvenance
dgn-np:NP311691.RAV0OgI3ejRSkT94CgXuVEzSmIKADNellQbDv9sp7K4yA130_provenance
;
np:hasPublicationInfo
dgn-np:NP311691.RAV0OgI3ejRSkT94CgXuVEzSmIKADNellQbDv9sp7K4yA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP311691.RAV0OgI3ejRSkT94CgXuVEzSmIKADNellQbDv9sp7K4yA130_assertion
a
np:Assertion
.
dgn-np:NP311691.RAV0OgI3ejRSkT94CgXuVEzSmIKADNellQbDv9sp7K4yA130_provenance
a
np:Provenance
.
dgn-np:NP311691.RAV0OgI3ejRSkT94CgXuVEzSmIKADNellQbDv9sp7K4yA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP311691.RAV0OgI3ejRSkT94CgXuVEzSmIKADNellQbDv9sp7K4yA130_assertion
{
miriam-gene:54657
a
ncit:C16612
.
lld:C0014544
a
ncit:C7057
.
dgn-gda:DGNb1541ea40172f971fba659c7696da732
sio:SIO_000628
miriam-gene:54657
,
lld:C0014544
;
a
sio:SIO_001121
.
}
dgn-np:NP311691.RAV0OgI3ejRSkT94CgXuVEzSmIKADNellQbDv9sp7K4yA130_provenance
{
dgn-np:NP311691.RAV0OgI3ejRSkT94CgXuVEzSmIKADNellQbDv9sp7K4yA130_assertion
dcterms:description
"[For those under treatment with LTG, UGT1A4 and UGT2B7 genotyping might be of clinical use and could contribute to the interindividual variability in LTG concentration to dose ratio in epileptic patients.]. 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:21557672
;
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:NP311691.RAV0OgI3ejRSkT94CgXuVEzSmIKADNellQbDv9sp7K4yA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:58+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" .
}