@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP401252.RAd9KWTI6QG-Em4xAmdTEAHyDhI6gZlu237wMP3WdfSnM
> .
@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:NP401252.RAd9KWTI6QG-Em4xAmdTEAHyDhI6gZlu237wMP3WdfSnM130_head
{
this:
np:hasAssertion
dgn-np:NP401252.RAd9KWTI6QG-Em4xAmdTEAHyDhI6gZlu237wMP3WdfSnM130_assertion
;
np:hasProvenance
dgn-np:NP401252.RAd9KWTI6QG-Em4xAmdTEAHyDhI6gZlu237wMP3WdfSnM130_provenance
;
np:hasPublicationInfo
dgn-np:NP401252.RAd9KWTI6QG-Em4xAmdTEAHyDhI6gZlu237wMP3WdfSnM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP401252.RAd9KWTI6QG-Em4xAmdTEAHyDhI6gZlu237wMP3WdfSnM130_assertion
a
np:Assertion
.
dgn-np:NP401252.RAd9KWTI6QG-Em4xAmdTEAHyDhI6gZlu237wMP3WdfSnM130_provenance
a
np:Provenance
.
dgn-np:NP401252.RAd9KWTI6QG-Em4xAmdTEAHyDhI6gZlu237wMP3WdfSnM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP401252.RAd9KWTI6QG-Em4xAmdTEAHyDhI6gZlu237wMP3WdfSnM130_assertion
{
miriam-gene:1565
a
ncit:C16612
.
lld:C0152115
a
ncit:C7057
.
dgn-gda:DGN6ae9b26c23c36713746a41f868c5f0c4
sio:SIO_000628
miriam-gene:1565
,
lld:C0152115
;
a
sio:SIO_001121
.
}
dgn-np:NP401252.RAd9KWTI6QG-Em4xAmdTEAHyDhI6gZlu237wMP3WdfSnM130_provenance
{
dgn-np:NP401252.RAd9KWTI6QG-Em4xAmdTEAHyDhI6gZlu237wMP3WdfSnM130_assertion
dcterms:description
"[As slight differences in the metabolism of drugs in patients heterozygous for CYP2D6 mutations and patients without such mutations are known, we conclude that heterozygous carriers of 2D6 mutated alleles may show an increased susceptibility to developing TD.]. 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:9713905
;
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:NP401252.RAd9KWTI6QG-Em4xAmdTEAHyDhI6gZlu237wMP3WdfSnM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:59+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" .
}