@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP238575.RAyvF2hNbTJBUJuANblhqIRlPtGd8Ahsymb_T0fewXLcM
> .
@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:NP238575.RAyvF2hNbTJBUJuANblhqIRlPtGd8Ahsymb_T0fewXLcM130_head
{
this:
np:hasAssertion
dgn-np:NP238575.RAyvF2hNbTJBUJuANblhqIRlPtGd8Ahsymb_T0fewXLcM130_assertion
;
np:hasProvenance
dgn-np:NP238575.RAyvF2hNbTJBUJuANblhqIRlPtGd8Ahsymb_T0fewXLcM130_provenance
;
np:hasPublicationInfo
dgn-np:NP238575.RAyvF2hNbTJBUJuANblhqIRlPtGd8Ahsymb_T0fewXLcM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP238575.RAyvF2hNbTJBUJuANblhqIRlPtGd8Ahsymb_T0fewXLcM130_assertion
a
np:Assertion
.
dgn-np:NP238575.RAyvF2hNbTJBUJuANblhqIRlPtGd8Ahsymb_T0fewXLcM130_provenance
a
np:Provenance
.
dgn-np:NP238575.RAyvF2hNbTJBUJuANblhqIRlPtGd8Ahsymb_T0fewXLcM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP238575.RAyvF2hNbTJBUJuANblhqIRlPtGd8Ahsymb_T0fewXLcM130_assertion
{
miriam-gene:3577
a
ncit:C16612
.
lld:C0011847
a
ncit:C7057
.
dgn-gda:DGNa11e52f29ebd60c2dc8b21cfd3691944
sio:SIO_000628
miriam-gene:3577
,
lld:C0011847
;
a
sio:SIO_001121
.
}
dgn-np:NP238575.RAyvF2hNbTJBUJuANblhqIRlPtGd8Ahsymb_T0fewXLcM130_provenance
{
dgn-np:NP238575.RAyvF2hNbTJBUJuANblhqIRlPtGd8Ahsymb_T0fewXLcM130_assertion
dcterms:description
"[The donor GA/AA genotypes of CXCR1 -2668G/A (rs2671222) were associated with increased risk for acute rejection even after adjusting for covariates such as gender, diabetes, preemptive transplantation, immunosuppressive regimen, relationship with the donor, and human leukocyte antigen mismatch (adjusted odds ratio 3.56; 95% confidence interval 1.37-9.27; P=0.009).]. 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:21452410
;
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:NP238575.RAyvF2hNbTJBUJuANblhqIRlPtGd8Ahsymb_T0fewXLcM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:13+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" .
}