@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP660390.RADqNI5gNoI-h1PMMD6NbexQ63ij5VQEQmbtK93nR4_As
> .
@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:NP660390.RADqNI5gNoI-h1PMMD6NbexQ63ij5VQEQmbtK93nR4_As130_head
{
this:
np:hasAssertion
dgn-np:NP660390.RADqNI5gNoI-h1PMMD6NbexQ63ij5VQEQmbtK93nR4_As130_assertion
;
np:hasProvenance
dgn-np:NP660390.RADqNI5gNoI-h1PMMD6NbexQ63ij5VQEQmbtK93nR4_As130_provenance
;
np:hasPublicationInfo
dgn-np:NP660390.RADqNI5gNoI-h1PMMD6NbexQ63ij5VQEQmbtK93nR4_As130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP660390.RADqNI5gNoI-h1PMMD6NbexQ63ij5VQEQmbtK93nR4_As130_assertion
a
np:Assertion
.
dgn-np:NP660390.RADqNI5gNoI-h1PMMD6NbexQ63ij5VQEQmbtK93nR4_As130_provenance
a
np:Provenance
.
dgn-np:NP660390.RADqNI5gNoI-h1PMMD6NbexQ63ij5VQEQmbtK93nR4_As130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP660390.RADqNI5gNoI-h1PMMD6NbexQ63ij5VQEQmbtK93nR4_As130_assertion
{
miriam-gene:5243
a
ncit:C16612
.
lld:C0036341
a
ncit:C7057
.
dgn-gda:DGN854ddae2e0129729d97645031ceac55e
sio:SIO_000628
miriam-gene:5243
,
lld:C0036341
;
a
sio:SIO_001121
.
}
dgn-np:NP660390.RADqNI5gNoI-h1PMMD6NbexQ63ij5VQEQmbtK93nR4_As130_provenance
{
dgn-np:NP660390.RADqNI5gNoI-h1PMMD6NbexQ63ij5VQEQmbtK93nR4_As130_assertion
dcterms:description
"[The impact of the UGT1A4, CYP1A2, and MDR1 genetic variants on olanzapine plasma levels, in relation to those of other individual factors, such as gender, smoking status, body weight, and age, was investigated in patients with schizophrenia.]. 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:20143052
;
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:NP660390.RADqNI5gNoI-h1PMMD6NbexQ63ij5VQEQmbtK93nR4_As130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:39+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" .
}