@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP367636.RAqEnpYr9ldFiCX0ty4DqhOf3iisRd2WfsKl2SdmgnrpM
> .
@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:NP367636.RAqEnpYr9ldFiCX0ty4DqhOf3iisRd2WfsKl2SdmgnrpM130_head
{
this:
np:hasAssertion
dgn-np:NP367636.RAqEnpYr9ldFiCX0ty4DqhOf3iisRd2WfsKl2SdmgnrpM130_assertion
;
np:hasProvenance
dgn-np:NP367636.RAqEnpYr9ldFiCX0ty4DqhOf3iisRd2WfsKl2SdmgnrpM130_provenance
;
np:hasPublicationInfo
dgn-np:NP367636.RAqEnpYr9ldFiCX0ty4DqhOf3iisRd2WfsKl2SdmgnrpM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP367636.RAqEnpYr9ldFiCX0ty4DqhOf3iisRd2WfsKl2SdmgnrpM130_assertion
a
np:Assertion
.
dgn-np:NP367636.RAqEnpYr9ldFiCX0ty4DqhOf3iisRd2WfsKl2SdmgnrpM130_provenance
a
np:Provenance
.
dgn-np:NP367636.RAqEnpYr9ldFiCX0ty4DqhOf3iisRd2WfsKl2SdmgnrpM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP367636.RAqEnpYr9ldFiCX0ty4DqhOf3iisRd2WfsKl2SdmgnrpM130_assertion
{
miriam-gene:6352
a
ncit:C16612
.
lld:C0027765
a
ncit:C7057
.
dgn-gda:DGN39454d761b1bc6bfba41e3e5969eadea
sio:SIO_000628
miriam-gene:6352
,
lld:C0027765
;
a
sio:SIO_001121
.
}
dgn-np:NP367636.RAqEnpYr9ldFiCX0ty4DqhOf3iisRd2WfsKl2SdmgnrpM130_provenance
{
dgn-np:NP367636.RAqEnpYr9ldFiCX0ty4DqhOf3iisRd2WfsKl2SdmgnrpM130_assertion
dcterms:description
"[As VE is a neurological disease characterized by the inflammatory reactions systematically observed in the spinocerebellar fluid and in the brain tissue of deceased patients, we examined 17 single nucleotide polymorphisms (SNPs) across seven inflammation-related candidate gene regions, including chemokine receptors type 2 and 5 (CCR2/CCR5), interferon-gamma (IFN-gamma), interleukin-4 (IL-4), IL-6, IL-10, stromal cell-derived factor (SDF) and chemokine regulated upon activation, normal T-cell expressed and presumably secreted (RANTES).]. 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:15182325
;
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:NP367636.RAqEnpYr9ldFiCX0ty4DqhOf3iisRd2WfsKl2SdmgnrpM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:35+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" .
}