@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP589239.RACMbjgIGyCl26owvTBcO3j5KO_IUvSRuJ4unM1zv89Kw
> .
@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:NP589239.RACMbjgIGyCl26owvTBcO3j5KO_IUvSRuJ4unM1zv89Kw130_head
{
this:
np:hasAssertion
dgn-np:NP589239.RACMbjgIGyCl26owvTBcO3j5KO_IUvSRuJ4unM1zv89Kw130_assertion
;
np:hasProvenance
dgn-np:NP589239.RACMbjgIGyCl26owvTBcO3j5KO_IUvSRuJ4unM1zv89Kw130_provenance
;
np:hasPublicationInfo
dgn-np:NP589239.RACMbjgIGyCl26owvTBcO3j5KO_IUvSRuJ4unM1zv89Kw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP589239.RACMbjgIGyCl26owvTBcO3j5KO_IUvSRuJ4unM1zv89Kw130_assertion
a
np:Assertion
.
dgn-np:NP589239.RACMbjgIGyCl26owvTBcO3j5KO_IUvSRuJ4unM1zv89Kw130_provenance
a
np:Provenance
.
dgn-np:NP589239.RACMbjgIGyCl26owvTBcO3j5KO_IUvSRuJ4unM1zv89Kw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP589239.RACMbjgIGyCl26owvTBcO3j5KO_IUvSRuJ4unM1zv89Kw130_assertion
{
miriam-gene:5743
a
ncit:C16612
.
lld:C0184567
a
ncit:C7057
.
dgn-gda:DGN5648083287d6b13970e6242ec0475011
sio:SIO_000628
miriam-gene:5743
,
lld:C0184567
;
a
sio:SIO_001121
.
}
dgn-np:NP589239.RACMbjgIGyCl26owvTBcO3j5KO_IUvSRuJ4unM1zv89Kw130_provenance
{
dgn-np:NP589239.RACMbjgIGyCl26owvTBcO3j5KO_IUvSRuJ4unM1zv89Kw130_assertion
dcterms:description
"[These results suggest that wide variability in gene expression and functional polymorphisms in PTGS2 may explain part of the interindividual variations in acute pain and the analgesic efficacy of nonsteroidal anti-inflammatory drugs and selective COX-2 inhibitors; this may be useful to define individual responders on the basis of genetic variations to predict patient risk and benefit to drugs.]. 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:16678543
;
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:NP589239.RACMbjgIGyCl26owvTBcO3j5KO_IUvSRuJ4unM1zv89Kw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:54+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" .
}