@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP884355.RAFIS9Ryui4nLOHY307cJyKznHGnmvbezY4h5UYilWt9w
> .
@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:NP884355.RAFIS9Ryui4nLOHY307cJyKznHGnmvbezY4h5UYilWt9w130_head
{
this:
np:hasAssertion
dgn-np:NP884355.RAFIS9Ryui4nLOHY307cJyKznHGnmvbezY4h5UYilWt9w130_assertion
;
np:hasProvenance
dgn-np:NP884355.RAFIS9Ryui4nLOHY307cJyKznHGnmvbezY4h5UYilWt9w130_provenance
;
np:hasPublicationInfo
dgn-np:NP884355.RAFIS9Ryui4nLOHY307cJyKznHGnmvbezY4h5UYilWt9w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP884355.RAFIS9Ryui4nLOHY307cJyKznHGnmvbezY4h5UYilWt9w130_assertion
a
np:Assertion
.
dgn-np:NP884355.RAFIS9Ryui4nLOHY307cJyKznHGnmvbezY4h5UYilWt9w130_provenance
a
np:Provenance
.
dgn-np:NP884355.RAFIS9Ryui4nLOHY307cJyKznHGnmvbezY4h5UYilWt9w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP884355.RAFIS9Ryui4nLOHY307cJyKznHGnmvbezY4h5UYilWt9w130_assertion
{
miriam-gene:1565
a
ncit:C16612
.
lld:C0040479
a
ncit:C7057
.
dgn-gda:DGN4238b7e65bc3d8aa7bfe997ccb3b7927
sio:SIO_000628
miriam-gene:1565
,
lld:C0040479
;
a
sio:SIO_001121
.
}
dgn-np:NP884355.RAFIS9Ryui4nLOHY307cJyKznHGnmvbezY4h5UYilWt9w130_provenance
{
dgn-np:NP884355.RAFIS9Ryui4nLOHY307cJyKznHGnmvbezY4h5UYilWt9w130_assertion
dcterms:description
"[Using the UK Yellow Card scheme to identify patients, blood samples were obtained from eight patients who survived ventricular tachycardia or torsades de pointes suspected to be due to terodiline, for determination of CYP2D6 and CYP2C19 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:10886124
;
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:NP884355.RAFIS9Ryui4nLOHY307cJyKznHGnmvbezY4h5UYilWt9w130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:00+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" .
}