@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP60000.RA20ofE_w8gUeZKShCm2A888ESTvUnRULWVnCRW9LguWg
> .
@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 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:NP60000.RA20ofE_w8gUeZKShCm2A888ESTvUnRULWVnCRW9LguWg130_head
{
this:
np:hasAssertion
dgn-np:NP60000.RA20ofE_w8gUeZKShCm2A888ESTvUnRULWVnCRW9LguWg130_assertion
;
np:hasProvenance
dgn-np:NP60000.RA20ofE_w8gUeZKShCm2A888ESTvUnRULWVnCRW9LguWg130_provenance
;
np:hasPublicationInfo
dgn-np:NP60000.RA20ofE_w8gUeZKShCm2A888ESTvUnRULWVnCRW9LguWg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP60000.RA20ofE_w8gUeZKShCm2A888ESTvUnRULWVnCRW9LguWg130_assertion
a
np:Assertion
.
dgn-np:NP60000.RA20ofE_w8gUeZKShCm2A888ESTvUnRULWVnCRW9LguWg130_provenance
a
np:Provenance
.
dgn-np:NP60000.RA20ofE_w8gUeZKShCm2A888ESTvUnRULWVnCRW9LguWg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP60000.RA20ofE_w8gUeZKShCm2A888ESTvUnRULWVnCRW9LguWg130_assertion
{
miriam-gene:1565
a
ncit:C16612
.
lld:C1527249
a
ncit:C7057
.
dgn-gda:DGNd0ca7834d3465cf7a71bafdd3ed701fc
sio:SIO_000628
miriam-gene:1565
,
lld:C1527249
;
a
sio:SIO_001122
.
}
dgn-np:NP60000.RA20ofE_w8gUeZKShCm2A888ESTvUnRULWVnCRW9LguWg130_provenance
{
dgn-np:NP60000.RA20ofE_w8gUeZKShCm2A888ESTvUnRULWVnCRW9LguWg130_assertion
dct:description
"[A CYP2D6 phenotype-genotype mismatch (phenocopying) can occur in Japanese psychiatric patients receiving clinical doses of some psychotropic drugs where the prevalence of PMs is low and the pharmacodynamic responses to those drugs are enhanced compared to Caucasian 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:14571354
;
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:NP60000.RA20ofE_w8gUeZKShCm2A888ESTvUnRULWVnCRW9LguWg130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:28+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}