@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP687580.RA3AZiZ-Kv4hVLh8qMpXBGE0DIiwsJB1RuNHHd-qe8hBI
> .
@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:NP687580.RA3AZiZ-Kv4hVLh8qMpXBGE0DIiwsJB1RuNHHd-qe8hBI130_head
{
this:
np:hasAssertion
dgn-np:NP687580.RA3AZiZ-Kv4hVLh8qMpXBGE0DIiwsJB1RuNHHd-qe8hBI130_assertion
;
np:hasProvenance
dgn-np:NP687580.RA3AZiZ-Kv4hVLh8qMpXBGE0DIiwsJB1RuNHHd-qe8hBI130_provenance
;
np:hasPublicationInfo
dgn-np:NP687580.RA3AZiZ-Kv4hVLh8qMpXBGE0DIiwsJB1RuNHHd-qe8hBI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP687580.RA3AZiZ-Kv4hVLh8qMpXBGE0DIiwsJB1RuNHHd-qe8hBI130_assertion
a
np:Assertion
.
dgn-np:NP687580.RA3AZiZ-Kv4hVLh8qMpXBGE0DIiwsJB1RuNHHd-qe8hBI130_provenance
a
np:Provenance
.
dgn-np:NP687580.RA3AZiZ-Kv4hVLh8qMpXBGE0DIiwsJB1RuNHHd-qe8hBI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP687580.RA3AZiZ-Kv4hVLh8qMpXBGE0DIiwsJB1RuNHHd-qe8hBI130_assertion
{
miriam-gene:5669
a
ncit:C16612
.
lld:C0007222
a
ncit:C7057
.
dgn-gda:DGN5f000636c785f99fab67af225bc9d8c2
sio:SIO_000628
miriam-gene:5669
,
lld:C0007222
;
a
sio:SIO_001121
.
}
dgn-np:NP687580.RA3AZiZ-Kv4hVLh8qMpXBGE0DIiwsJB1RuNHHd-qe8hBI130_provenance
{
dgn-np:NP687580.RA3AZiZ-Kv4hVLh8qMpXBGE0DIiwsJB1RuNHHd-qe8hBI130_assertion
dcterms:description
"[Analysis of functional modules revealed the possible regulatory roles of SP1 and CXCL12 in the pathogenesis of cardiovascular disease (CVD) and modulation of their activities may be considered as potential therapeutic tools.]. 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:21559538
;
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:NP687580.RA3AZiZ-Kv4hVLh8qMpXBGE0DIiwsJB1RuNHHd-qe8hBI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:58+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" .
}