@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP278663.RACm_feJ3mRBtvKsd_uurxtcNwCf4xIRXVZhCKQSOqgjY
> .
@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:NP278663.RACm_feJ3mRBtvKsd_uurxtcNwCf4xIRXVZhCKQSOqgjY130_head
{
this:
np:hasAssertion
dgn-np:NP278663.RACm_feJ3mRBtvKsd_uurxtcNwCf4xIRXVZhCKQSOqgjY130_assertion
;
np:hasProvenance
dgn-np:NP278663.RACm_feJ3mRBtvKsd_uurxtcNwCf4xIRXVZhCKQSOqgjY130_provenance
;
np:hasPublicationInfo
dgn-np:NP278663.RACm_feJ3mRBtvKsd_uurxtcNwCf4xIRXVZhCKQSOqgjY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP278663.RACm_feJ3mRBtvKsd_uurxtcNwCf4xIRXVZhCKQSOqgjY130_assertion
a
np:Assertion
.
dgn-np:NP278663.RACm_feJ3mRBtvKsd_uurxtcNwCf4xIRXVZhCKQSOqgjY130_provenance
a
np:Provenance
.
dgn-np:NP278663.RACm_feJ3mRBtvKsd_uurxtcNwCf4xIRXVZhCKQSOqgjY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP278663.RACm_feJ3mRBtvKsd_uurxtcNwCf4xIRXVZhCKQSOqgjY130_assertion
{
miriam-gene:2811
a
ncit:C16612
.
lld:C1956346
a
ncit:C7057
.
dgn-gda:DGN875bbb716677b0ee2d0537f79337da25
sio:SIO_000628
miriam-gene:2811
,
lld:C1956346
;
a
sio:SIO_001121
.
}
dgn-np:NP278663.RACm_feJ3mRBtvKsd_uurxtcNwCf4xIRXVZhCKQSOqgjY130_provenance
{
dgn-np:NP278663.RACm_feJ3mRBtvKsd_uurxtcNwCf4xIRXVZhCKQSOqgjY130_assertion
dcterms:description
"[SNP rs10757278 on chromosome 9 was genotyped in 926 patients with CAD from the CAREGENE study, in 648 patients with CVD from the Leuven Stroke Genetics Study (LSGS) and the Belgian Stroke Study (BSS) and in 828 unrelated controls.]. 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:19319159
;
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:NP278663.RACm_feJ3mRBtvKsd_uurxtcNwCf4xIRXVZhCKQSOqgjY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:37+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" .
}