@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP856448.RARLGkoPM_gvYHCDYKG8Pyj9hMZFK91iXgT8uqY0W17SM
> .
@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:NP856448.RARLGkoPM_gvYHCDYKG8Pyj9hMZFK91iXgT8uqY0W17SM130_head
{
this:
np:hasAssertion
dgn-np:NP856448.RARLGkoPM_gvYHCDYKG8Pyj9hMZFK91iXgT8uqY0W17SM130_assertion
;
np:hasProvenance
dgn-np:NP856448.RARLGkoPM_gvYHCDYKG8Pyj9hMZFK91iXgT8uqY0W17SM130_provenance
;
np:hasPublicationInfo
dgn-np:NP856448.RARLGkoPM_gvYHCDYKG8Pyj9hMZFK91iXgT8uqY0W17SM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP856448.RARLGkoPM_gvYHCDYKG8Pyj9hMZFK91iXgT8uqY0W17SM130_assertion
a
np:Assertion
.
dgn-np:NP856448.RARLGkoPM_gvYHCDYKG8Pyj9hMZFK91iXgT8uqY0W17SM130_provenance
a
np:Provenance
.
dgn-np:NP856448.RARLGkoPM_gvYHCDYKG8Pyj9hMZFK91iXgT8uqY0W17SM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP856448.RARLGkoPM_gvYHCDYKG8Pyj9hMZFK91iXgT8uqY0W17SM130_assertion
{
miriam-gene:5972
a
ncit:C16612
.
lld:C2733158
a
ncit:C7057
.
dgn-gda:DGNfea69c032841e14334f4b2411dd3a70e
sio:SIO_000628
miriam-gene:5972
,
lld:C2733158
;
a
sio:SIO_001121
.
}
dgn-np:NP856448.RARLGkoPM_gvYHCDYKG8Pyj9hMZFK91iXgT8uqY0W17SM130_provenance
{
dgn-np:NP856448.RARLGkoPM_gvYHCDYKG8Pyj9hMZFK91iXgT8uqY0W17SM130_assertion
dcterms:description
"[Genetic association studies in the setting of the Austrian Stroke Prevention Study described that polymorphisms in the renin angiotensin system (RAS) increase the susceptibility for progression of cerebral small vessel disease.]. 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:12456049
;
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:NP856448.RARLGkoPM_gvYHCDYKG8Pyj9hMZFK91iXgT8uqY0W17SM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:43+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" .
}