@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP91843.RAyBSE8dnnjsxOAJG3RRlGm0H7YSRNAyo7sTfNf3_rjRc
> .
@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:NP91843.RAyBSE8dnnjsxOAJG3RRlGm0H7YSRNAyo7sTfNf3_rjRc130_head
{
this:
np:hasAssertion
dgn-np:NP91843.RAyBSE8dnnjsxOAJG3RRlGm0H7YSRNAyo7sTfNf3_rjRc130_assertion
;
np:hasProvenance
dgn-np:NP91843.RAyBSE8dnnjsxOAJG3RRlGm0H7YSRNAyo7sTfNf3_rjRc130_provenance
;
np:hasPublicationInfo
dgn-np:NP91843.RAyBSE8dnnjsxOAJG3RRlGm0H7YSRNAyo7sTfNf3_rjRc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP91843.RAyBSE8dnnjsxOAJG3RRlGm0H7YSRNAyo7sTfNf3_rjRc130_assertion
a
np:Assertion
.
dgn-np:NP91843.RAyBSE8dnnjsxOAJG3RRlGm0H7YSRNAyo7sTfNf3_rjRc130_provenance
a
np:Provenance
.
dgn-np:NP91843.RAyBSE8dnnjsxOAJG3RRlGm0H7YSRNAyo7sTfNf3_rjRc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP91843.RAyBSE8dnnjsxOAJG3RRlGm0H7YSRNAyo7sTfNf3_rjRc130_assertion
{
miriam-gene:7099
a
ncit:C16612
.
lld:C0948480
a
ncit:C7057
.
dgn-gda:DGN3af8cb589c793c136811a9334f95337a
sio:SIO_000628
miriam-gene:7099
,
lld:C0948480
;
a
sio:SIO_001122
.
}
dgn-np:NP91843.RAyBSE8dnnjsxOAJG3RRlGm0H7YSRNAyo7sTfNf3_rjRc130_provenance
{
dgn-np:NP91843.RAyBSE8dnnjsxOAJG3RRlGm0H7YSRNAyo7sTfNf3_rjRc130_assertion
dcterms:description
"[Although inflammation has been implicated in the pathophysiology of restenosis, the 896A/G and 1196C/T polymorphisms or haplotypes based on these polymorphisms at the TLR4 locus are not associated with an increased risk of target vessel revascularization or angiographic restenosis after PCI. These polymorphisms are not useful for pre-PCI identification of patients at risk for restenosis.]. 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:20671584
;
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:NP91843.RAyBSE8dnnjsxOAJG3RRlGm0H7YSRNAyo7sTfNf3_rjRc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:45+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" .
}