@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP308765.RAHyvQvZZqL1dIwrhjYi__vUgifDyvvx6HzlCAcXGTspU
> .
@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:NP308765.RAHyvQvZZqL1dIwrhjYi__vUgifDyvvx6HzlCAcXGTspU130_head
{
this:
np:hasAssertion
dgn-np:NP308765.RAHyvQvZZqL1dIwrhjYi__vUgifDyvvx6HzlCAcXGTspU130_assertion
;
np:hasProvenance
dgn-np:NP308765.RAHyvQvZZqL1dIwrhjYi__vUgifDyvvx6HzlCAcXGTspU130_provenance
;
np:hasPublicationInfo
dgn-np:NP308765.RAHyvQvZZqL1dIwrhjYi__vUgifDyvvx6HzlCAcXGTspU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP308765.RAHyvQvZZqL1dIwrhjYi__vUgifDyvvx6HzlCAcXGTspU130_assertion
a
np:Assertion
.
dgn-np:NP308765.RAHyvQvZZqL1dIwrhjYi__vUgifDyvvx6HzlCAcXGTspU130_provenance
a
np:Provenance
.
dgn-np:NP308765.RAHyvQvZZqL1dIwrhjYi__vUgifDyvvx6HzlCAcXGTspU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP308765.RAHyvQvZZqL1dIwrhjYi__vUgifDyvvx6HzlCAcXGTspU130_assertion
{
miriam-gene:183
a
ncit:C16612
.
lld:C0004153
a
ncit:C7057
.
dgn-gda:DGN9d023866cedbe1f8612f97410842ebff
sio:SIO_000628
miriam-gene:183
,
lld:C0004153
;
a
sio:SIO_001121
.
}
dgn-np:NP308765.RAHyvQvZZqL1dIwrhjYi__vUgifDyvvx6HzlCAcXGTspU130_provenance
{
dgn-np:NP308765.RAHyvQvZZqL1dIwrhjYi__vUgifDyvvx6HzlCAcXGTspU130_assertion
dcterms:description
"[Elevated levels of crosslinked AT1 receptor dimers on monocytes could sustain the process of atherogenesis, because inhibition of angiotensin II generation or of intracellular factor XIIIA activity suppressed the appearance of crosslinked AT1 receptors and symptoms of atherosclerosis in ApoE-deficient mice.]. 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:15507206
;
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:NP308765.RAHyvQvZZqL1dIwrhjYi__vUgifDyvvx6HzlCAcXGTspU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:57+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" .
}