@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP453325.RAPj-2ae53-5YTXb1UMs7eLaSkpAqLTdWA8jr9Tpm83mc
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP453325.RAPj-2ae53-5YTXb1UMs7eLaSkpAqLTdWA8jr9Tpm83mc130_assertion
;
np:hasProvenance
dgn-np:NP453325.RAPj-2ae53-5YTXb1UMs7eLaSkpAqLTdWA8jr9Tpm83mc130_provenance
;
np:hasPublicationInfo
dgn-np:NP453325.RAPj-2ae53-5YTXb1UMs7eLaSkpAqLTdWA8jr9Tpm83mc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP453325.RAPj-2ae53-5YTXb1UMs7eLaSkpAqLTdWA8jr9Tpm83mc130_assertion
a
np:Assertion
.
dgn-np:NP453325.RAPj-2ae53-5YTXb1UMs7eLaSkpAqLTdWA8jr9Tpm83mc130_provenance
a
np:Provenance
.
dgn-np:NP453325.RAPj-2ae53-5YTXb1UMs7eLaSkpAqLTdWA8jr9Tpm83mc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP453325.RAPj-2ae53-5YTXb1UMs7eLaSkpAqLTdWA8jr9Tpm83mc130_assertion
{
miriam-gene:1559
a
ncit:C16612
.
lld:C0014544
a
ncit:C7057
.
dgn-gda:DGN36de6c955bde4ca319b560b6ea718121
sio:SIO_000628
miriam-gene:1559
,
lld:C0014544
;
a
sio:SIO_001121
.
}
dgn-np:NP453325.RAPj-2ae53-5YTXb1UMs7eLaSkpAqLTdWA8jr9Tpm83mc130_provenance
{
dgn-np:NP453325.RAPj-2ae53-5YTXb1UMs7eLaSkpAqLTdWA8jr9Tpm83mc130_assertion
dcterms:description
"[We examined the contribution of CYP2C9 and CYP2C19 genotypes and drug interactions to the phenytoin metabolism among 97 Korean epileptic patients to determine if pharmacogenetic testing could be utilized in routine clinical practice.]. 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:17562299
;
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:NP453325.RAPj-2ae53-5YTXb1UMs7eLaSkpAqLTdWA8jr9Tpm83mc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:30+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
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}