@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP557785.RACmBIjOliejdiqc5468ACi2_kkb5DclN31LqVgTye5Ns
> .
@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:NP557785.RACmBIjOliejdiqc5468ACi2_kkb5DclN31LqVgTye5Ns130_head
{
this:
np:hasAssertion
dgn-np:NP557785.RACmBIjOliejdiqc5468ACi2_kkb5DclN31LqVgTye5Ns130_assertion
;
np:hasProvenance
dgn-np:NP557785.RACmBIjOliejdiqc5468ACi2_kkb5DclN31LqVgTye5Ns130_provenance
;
np:hasPublicationInfo
dgn-np:NP557785.RACmBIjOliejdiqc5468ACi2_kkb5DclN31LqVgTye5Ns130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP557785.RACmBIjOliejdiqc5468ACi2_kkb5DclN31LqVgTye5Ns130_assertion
a
np:Assertion
.
dgn-np:NP557785.RACmBIjOliejdiqc5468ACi2_kkb5DclN31LqVgTye5Ns130_provenance
a
np:Provenance
.
dgn-np:NP557785.RACmBIjOliejdiqc5468ACi2_kkb5DclN31LqVgTye5Ns130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP557785.RACmBIjOliejdiqc5468ACi2_kkb5DclN31LqVgTye5Ns130_assertion
{
miriam-gene:6667
a
ncit:C16612
.
lld:C0019061
a
ncit:C7057
.
dgn-gda:DGNa74ecd84bf9f33ce04808d3c41a31dd5
sio:SIO_000628
miriam-gene:6667
,
lld:C0019061
;
a
sio:SIO_001121
.
}
dgn-np:NP557785.RACmBIjOliejdiqc5468ACi2_kkb5DclN31LqVgTye5Ns130_provenance
{
dgn-np:NP557785.RACmBIjOliejdiqc5468ACi2_kkb5DclN31LqVgTye5Ns130_assertion
dcterms:description
"[Since Sp1 is an inducer of several genes in the presence of the inflammatory cytokines in EC, our results suggest that the transcriptional regulation of the Gb3S gene by Sp1 might affect the VT sensitivity of EC and HUS progression.]. 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:18757779
;
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:NP557785.RACmBIjOliejdiqc5468ACi2_kkb5DclN31LqVgTye5Ns130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:36+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" .
}