@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP45814.RASMne6p3qDnULYmuAvfchwFUnoYe2WfPSEQ70ZDuA3L0
> .
@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:NP45814.RASMne6p3qDnULYmuAvfchwFUnoYe2WfPSEQ70ZDuA3L0130_head
{
this:
np:hasAssertion
dgn-np:NP45814.RASMne6p3qDnULYmuAvfchwFUnoYe2WfPSEQ70ZDuA3L0130_assertion
;
np:hasProvenance
dgn-np:NP45814.RASMne6p3qDnULYmuAvfchwFUnoYe2WfPSEQ70ZDuA3L0130_provenance
;
np:hasPublicationInfo
dgn-np:NP45814.RASMne6p3qDnULYmuAvfchwFUnoYe2WfPSEQ70ZDuA3L0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP45814.RASMne6p3qDnULYmuAvfchwFUnoYe2WfPSEQ70ZDuA3L0130_assertion
a
np:Assertion
.
dgn-np:NP45814.RASMne6p3qDnULYmuAvfchwFUnoYe2WfPSEQ70ZDuA3L0130_provenance
a
np:Provenance
.
dgn-np:NP45814.RASMne6p3qDnULYmuAvfchwFUnoYe2WfPSEQ70ZDuA3L0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP45814.RASMne6p3qDnULYmuAvfchwFUnoYe2WfPSEQ70ZDuA3L0130_assertion
{
miriam-gene:1557
a
ncit:C16612
.
lld:C0038354
a
ncit:C7057
.
dgn-gda:DGN1b66d57739dfb7e4cefacc8ecde75c6e
sio:SIO_000628
miriam-gene:1557
,
lld:C0038354
;
a
sio:SIO_001122
.
}
dgn-np:NP45814.RASMne6p3qDnULYmuAvfchwFUnoYe2WfPSEQ70ZDuA3L0130_provenance
{
dgn-np:NP45814.RASMne6p3qDnULYmuAvfchwFUnoYe2WfPSEQ70ZDuA3L0130_assertion
dcterms:description
"[We suggest that the reason why the wt/wt had high concentrations of omeprazole similar to those in the other two genotype groups is that some of them were old with low CYP2C19 activity. In these patients omeprazole accumulated from the first to the eighth dose similar to that in the heterozygotes.]. 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:15447734
;
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:NP45814.RASMne6p3qDnULYmuAvfchwFUnoYe2WfPSEQ70ZDuA3L0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:21+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" .
}