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http://rdf.disgenet.org/nanopublications.trig#NP236724.RAuO8otX4PNC0vpXEQtLzl09vxtBNcxoLVUNhEeMhev5w
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP236724.RAuO8otX4PNC0vpXEQtLzl09vxtBNcxoLVUNhEeMhev5w130_assertion
;
np:hasProvenance
dgn-np:NP236724.RAuO8otX4PNC0vpXEQtLzl09vxtBNcxoLVUNhEeMhev5w130_provenance
;
np:hasPublicationInfo
dgn-np:NP236724.RAuO8otX4PNC0vpXEQtLzl09vxtBNcxoLVUNhEeMhev5w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP236724.RAuO8otX4PNC0vpXEQtLzl09vxtBNcxoLVUNhEeMhev5w130_assertion
a
np:Assertion
.
dgn-np:NP236724.RAuO8otX4PNC0vpXEQtLzl09vxtBNcxoLVUNhEeMhev5w130_provenance
a
np:Provenance
.
dgn-np:NP236724.RAuO8otX4PNC0vpXEQtLzl09vxtBNcxoLVUNhEeMhev5w130_publicationInfo
a
np:PublicationInfo
.
}
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{
miriam-gene:3576
a
ncit:C16612
.
lld:C0015672
a
ncit:C7057
.
dgn-gda:DGN42e06e6dd7a61d512eef544a057d52a2
sio:SIO_000628
miriam-gene:3576
,
lld:C0015672
;
a
sio:SIO_001121
.
}
dgn-np:NP236724.RAuO8otX4PNC0vpXEQtLzl09vxtBNcxoLVUNhEeMhev5w130_provenance
{
dgn-np:NP236724.RAuO8otX4PNC0vpXEQtLzl09vxtBNcxoLVUNhEeMhev5w130_assertion
dcterms:description
"[Logistic regression analyses showed that after controlling for epidemiologic (age and sex), clinical (stage of disease, comorbidities), and symptom (depressed mood and fatigue) variables known to influence pain severity, variant alleles in IL-8 -251T/A [odds ratio (OR), 2.35; 95% confidence interval (95% CI), 1.10-5.03; P = 0.03] persisted as a significant factor for severe pain for White patients.]. 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:18086782
;
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:NP236724.RAuO8otX4PNC0vpXEQtLzl09vxtBNcxoLVUNhEeMhev5w130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:12+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" .
}