@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP591864.RAg7z9hbUK3DrxtPJVbplbRz6CQt9WFnqicF7Dk87GEcM
> .
@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:NP591864.RAg7z9hbUK3DrxtPJVbplbRz6CQt9WFnqicF7Dk87GEcM130_head
{
this:
np:hasAssertion
dgn-np:NP591864.RAg7z9hbUK3DrxtPJVbplbRz6CQt9WFnqicF7Dk87GEcM130_assertion
;
np:hasProvenance
dgn-np:NP591864.RAg7z9hbUK3DrxtPJVbplbRz6CQt9WFnqicF7Dk87GEcM130_provenance
;
np:hasPublicationInfo
dgn-np:NP591864.RAg7z9hbUK3DrxtPJVbplbRz6CQt9WFnqicF7Dk87GEcM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP591864.RAg7z9hbUK3DrxtPJVbplbRz6CQt9WFnqicF7Dk87GEcM130_assertion
a
np:Assertion
.
dgn-np:NP591864.RAg7z9hbUK3DrxtPJVbplbRz6CQt9WFnqicF7Dk87GEcM130_provenance
a
np:Provenance
.
dgn-np:NP591864.RAg7z9hbUK3DrxtPJVbplbRz6CQt9WFnqicF7Dk87GEcM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP591864.RAg7z9hbUK3DrxtPJVbplbRz6CQt9WFnqicF7Dk87GEcM130_assertion
{
miriam-gene:3769
a
ncit:C16612
.
lld:C3272363
a
ncit:C7057
.
dgn-gda:DGN468e8b7e85ae85c516199665ad55f731
sio:SIO_000628
miriam-gene:3769
,
lld:C3272363
;
a
sio:SIO_001121
.
}
dgn-np:NP591864.RAg7z9hbUK3DrxtPJVbplbRz6CQt9WFnqicF7Dk87GEcM130_provenance
{
dgn-np:NP591864.RAg7z9hbUK3DrxtPJVbplbRz6CQt9WFnqicF7Dk87GEcM130_assertion
dcterms:description
"[For the first time to our knowledge, we report this association not only for LVD and SVD but also for cryptogenic stroke, implying that future studies of the genetics of ischemic stroke should target these 3 subtypes.]. 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:15933254
;
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:NP591864.RAg7z9hbUK3DrxtPJVbplbRz6CQt9WFnqicF7Dk87GEcM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:56+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" .
}