@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP45813.RAhWU2GY59fPaSSfNSLL-wRAWoFyH7bYvBo96x--xjGro
> .
@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 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:NP45813.RAhWU2GY59fPaSSfNSLL-wRAWoFyH7bYvBo96x--xjGro130_head
{
this:
np:hasAssertion
dgn-np:NP45813.RAhWU2GY59fPaSSfNSLL-wRAWoFyH7bYvBo96x--xjGro130_assertion
;
np:hasProvenance
dgn-np:NP45813.RAhWU2GY59fPaSSfNSLL-wRAWoFyH7bYvBo96x--xjGro130_provenance
;
np:hasPublicationInfo
dgn-np:NP45813.RAhWU2GY59fPaSSfNSLL-wRAWoFyH7bYvBo96x--xjGro130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP45813.RAhWU2GY59fPaSSfNSLL-wRAWoFyH7bYvBo96x--xjGro130_assertion
a
np:Assertion
.
dgn-np:NP45813.RAhWU2GY59fPaSSfNSLL-wRAWoFyH7bYvBo96x--xjGro130_provenance
a
np:Provenance
.
dgn-np:NP45813.RAhWU2GY59fPaSSfNSLL-wRAWoFyH7bYvBo96x--xjGro130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP45813.RAhWU2GY59fPaSSfNSLL-wRAWoFyH7bYvBo96x--xjGro130_assertion
{
miriam-gene:1557
a
ncit:C16612
.
lld:C0038354
a
ncit:C7057
.
dgn-gda:DGNdc35a94de21e849f921ff9e83238d6e4
sio:SIO_000628
miriam-gene:1557
,
lld:C0038354
;
a
sio:SIO_001122
.
}
dgn-np:NP45813.RAhWU2GY59fPaSSfNSLL-wRAWoFyH7bYvBo96x--xjGro130_provenance
{
dgn-np:NP45813.RAhWU2GY59fPaSSfNSLL-wRAWoFyH7bYvBo96x--xjGro130_assertion
dct:description
"[ The combination regimen of famotidine plus rabeprazole is more effective for nocturnal acid inhibition in homozygous and heterozygous EMs than the increased dosage regimen of rabeprazole. This concomitant therapy could be a rescue regimen for patients with nocturnal acid breakthrough refractory to a standard PPI therapy who are likely to be CYP2C19 EMs.]. 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:15903128
;
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:NP45813.RAhWU2GY59fPaSSfNSLL-wRAWoFyH7bYvBo96x--xjGro130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:21+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}