@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP44618.RAuwNKSeN1CHYjgKD8LRNwSbeOa0qU1Tv0t1zSZWOS0I0
> .
@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 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:NP44618.RAuwNKSeN1CHYjgKD8LRNwSbeOa0qU1Tv0t1zSZWOS0I0130_head
{
this:
np:hasAssertion
dgn-np:NP44618.RAuwNKSeN1CHYjgKD8LRNwSbeOa0qU1Tv0t1zSZWOS0I0130_assertion
;
np:hasProvenance
dgn-np:NP44618.RAuwNKSeN1CHYjgKD8LRNwSbeOa0qU1Tv0t1zSZWOS0I0130_provenance
;
np:hasPublicationInfo
dgn-np:NP44618.RAuwNKSeN1CHYjgKD8LRNwSbeOa0qU1Tv0t1zSZWOS0I0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP44618.RAuwNKSeN1CHYjgKD8LRNwSbeOa0qU1Tv0t1zSZWOS0I0130_assertion
a
np:Assertion
.
dgn-np:NP44618.RAuwNKSeN1CHYjgKD8LRNwSbeOa0qU1Tv0t1zSZWOS0I0130_provenance
a
np:Provenance
.
dgn-np:NP44618.RAuwNKSeN1CHYjgKD8LRNwSbeOa0qU1Tv0t1zSZWOS0I0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP44618.RAuwNKSeN1CHYjgKD8LRNwSbeOa0qU1Tv0t1zSZWOS0I0130_assertion
{
miriam-gene:2162
a
ncit:C16612
.
lld:C0948008
a
ncit:C7057
.
dgn-gda:DGN6760f4216477306f84131d58ceda3edd
sio:SIO_000628
miriam-gene:2162
,
lld:C0948008
;
a
sio:SIO_001122
.
}
dgn-np:NP44618.RAuwNKSeN1CHYjgKD8LRNwSbeOa0qU1Tv0t1zSZWOS0I0130_provenance
{
dgn-np:NP44618.RAuwNKSeN1CHYjgKD8LRNwSbeOa0qU1Tv0t1zSZWOS0I0130_assertion
dct:description
"[There is a genetic component to common stroke. No single gene with major effect was identified; rather, common variants in several genes, each exerting a modest effect, contribute to the risk of stroke. These findings have important implications for the design of future genetic studies and for predictive genetic testing for stroke and other multifactorial diseases.]. 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:15534175
;
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:NP44618.RAuwNKSeN1CHYjgKD8LRNwSbeOa0qU1Tv0t1zSZWOS0I0130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:20+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}