@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP89686.RA5f62qpjiVxEt1F6_PjuDSvdLnuxF_d1SnWFJwLzHVhE
> .
@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:NP89686.RA5f62qpjiVxEt1F6_PjuDSvdLnuxF_d1SnWFJwLzHVhE130_head
{
this:
np:hasAssertion
dgn-np:NP89686.RA5f62qpjiVxEt1F6_PjuDSvdLnuxF_d1SnWFJwLzHVhE130_assertion
;
np:hasProvenance
dgn-np:NP89686.RA5f62qpjiVxEt1F6_PjuDSvdLnuxF_d1SnWFJwLzHVhE130_provenance
;
np:hasPublicationInfo
dgn-np:NP89686.RA5f62qpjiVxEt1F6_PjuDSvdLnuxF_d1SnWFJwLzHVhE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP89686.RA5f62qpjiVxEt1F6_PjuDSvdLnuxF_d1SnWFJwLzHVhE130_assertion
a
np:Assertion
.
dgn-np:NP89686.RA5f62qpjiVxEt1F6_PjuDSvdLnuxF_d1SnWFJwLzHVhE130_provenance
a
np:Provenance
.
dgn-np:NP89686.RA5f62qpjiVxEt1F6_PjuDSvdLnuxF_d1SnWFJwLzHVhE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP89686.RA5f62qpjiVxEt1F6_PjuDSvdLnuxF_d1SnWFJwLzHVhE130_assertion
{
miriam-gene:255738
a
ncit:C16612
.
lld:C0004153
a
ncit:C7057
.
dgn-gda:DGNee4e9708786c521f0badcd1523cfe03e
sio:SIO_000628
miriam-gene:255738
,
lld:C0004153
;
a
sio:SIO_001122
.
}
dgn-np:NP89686.RA5f62qpjiVxEt1F6_PjuDSvdLnuxF_d1SnWFJwLzHVhE130_provenance
{
dgn-np:NP89686.RA5f62qpjiVxEt1F6_PjuDSvdLnuxF_d1SnWFJwLzHVhE130_assertion
dcterms:description
"[Our findings in this unique combination of clinical and autopsy data, provide evidence that PCSK9 gene associates with the risk of LVA stroke subtype, and suggest that the risk is mediated by the severity of intracranial atherosclerosis.]. 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:17940607
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP89686.RA5f62qpjiVxEt1F6_PjuDSvdLnuxF_d1SnWFJwLzHVhE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:44+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" .
}