@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP77151.RApZXkT-yGYR9bwzQwamwhv9gBlbTxVOAYPDkcu5p7sok
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP77151.RApZXkT-yGYR9bwzQwamwhv9gBlbTxVOAYPDkcu5p7sok130_head
{
this:
np:hasAssertion
dgn-np:NP77151.RApZXkT-yGYR9bwzQwamwhv9gBlbTxVOAYPDkcu5p7sok130_assertion
;
np:hasProvenance
dgn-np:NP77151.RApZXkT-yGYR9bwzQwamwhv9gBlbTxVOAYPDkcu5p7sok130_provenance
;
np:hasPublicationInfo
dgn-np:NP77151.RApZXkT-yGYR9bwzQwamwhv9gBlbTxVOAYPDkcu5p7sok130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP77151.RApZXkT-yGYR9bwzQwamwhv9gBlbTxVOAYPDkcu5p7sok130_assertion
a
np:Assertion
.
dgn-np:NP77151.RApZXkT-yGYR9bwzQwamwhv9gBlbTxVOAYPDkcu5p7sok130_provenance
a
np:Provenance
.
dgn-np:NP77151.RApZXkT-yGYR9bwzQwamwhv9gBlbTxVOAYPDkcu5p7sok130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP77151.RApZXkT-yGYR9bwzQwamwhv9gBlbTxVOAYPDkcu5p7sok130_assertion
{
miriam-gene:1565
a
ncit:C16612
.
lld:C0011570
a
ncit:C7057
.
dgn-gda:DGNd99ca8e289ec58410246f1584fbcae33
sio:SIO_000628
miriam-gene:1565
,
lld:C0011570
;
a
sio:SIO_001122
.
}
dgn-np:NP77151.RApZXkT-yGYR9bwzQwamwhv9gBlbTxVOAYPDkcu5p7sok130_provenance
{
dgn-np:NP77151.RApZXkT-yGYR9bwzQwamwhv9gBlbTxVOAYPDkcu5p7sok130_assertion
dcterms:description
"[ Combined pharmacogenetic testing for CYP2D6 and CYP2C19 identifies patients with low risk for side effects in amitriptyline therapy and could possibly be used to individualize antidepressive regimens and reduce treatment cost. Identification of genotypes]. 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:15590749
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP77151.RApZXkT-yGYR9bwzQwamwhv9gBlbTxVOAYPDkcu5p7sok130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:22+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}