@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP870361.RALF-78tXbtOv-NABggvL8EaPwwu7qqdfgd5ZkJow1JAM
> .
@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:NP870361.RALF-78tXbtOv-NABggvL8EaPwwu7qqdfgd5ZkJow1JAM130_head
{
this:
np:hasAssertion
dgn-np:NP870361.RALF-78tXbtOv-NABggvL8EaPwwu7qqdfgd5ZkJow1JAM130_assertion
;
np:hasProvenance
dgn-np:NP870361.RALF-78tXbtOv-NABggvL8EaPwwu7qqdfgd5ZkJow1JAM130_provenance
;
np:hasPublicationInfo
dgn-np:NP870361.RALF-78tXbtOv-NABggvL8EaPwwu7qqdfgd5ZkJow1JAM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP870361.RALF-78tXbtOv-NABggvL8EaPwwu7qqdfgd5ZkJow1JAM130_assertion
a
np:Assertion
.
dgn-np:NP870361.RALF-78tXbtOv-NABggvL8EaPwwu7qqdfgd5ZkJow1JAM130_provenance
a
np:Provenance
.
dgn-np:NP870361.RALF-78tXbtOv-NABggvL8EaPwwu7qqdfgd5ZkJow1JAM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP870361.RALF-78tXbtOv-NABggvL8EaPwwu7qqdfgd5ZkJow1JAM130_assertion
{
miriam-gene:1565
a
ncit:C16612
.
lld:C0011265
a
ncit:C7057
.
dgn-gda:DGNe0e15db287d28d975ba7f88ee05e2c51
sio:SIO_000628
miriam-gene:1565
,
lld:C0011265
;
a
sio:SIO_001121
.
}
dgn-np:NP870361.RALF-78tXbtOv-NABggvL8EaPwwu7qqdfgd5ZkJow1JAM130_provenance
{
dgn-np:NP870361.RALF-78tXbtOv-NABggvL8EaPwwu7qqdfgd5ZkJow1JAM130_assertion
dcterms:description
"[The goal of this pilot study was to assess the feasibility of in vivo phenotyping of CYP2D6 in an elderly population with dementia and to determine if part of the variability in response to treatment with galantamine is attributable to CYP2D6 phenotype.]. 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:21803659
;
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:NP870361.RALF-78tXbtOv-NABggvL8EaPwwu7qqdfgd5ZkJow1JAM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:52+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" .
}