@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP292118.RAcUkfR-gv5AOIA0TWI_do4366v6-3ZSx5r1e-r7M-Psk
> .
@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:NP292118.RAcUkfR-gv5AOIA0TWI_do4366v6-3ZSx5r1e-r7M-Psk130_head
{
this:
np:hasAssertion
dgn-np:NP292118.RAcUkfR-gv5AOIA0TWI_do4366v6-3ZSx5r1e-r7M-Psk130_assertion
;
np:hasProvenance
dgn-np:NP292118.RAcUkfR-gv5AOIA0TWI_do4366v6-3ZSx5r1e-r7M-Psk130_provenance
;
np:hasPublicationInfo
dgn-np:NP292118.RAcUkfR-gv5AOIA0TWI_do4366v6-3ZSx5r1e-r7M-Psk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP292118.RAcUkfR-gv5AOIA0TWI_do4366v6-3ZSx5r1e-r7M-Psk130_assertion
a
np:Assertion
.
dgn-np:NP292118.RAcUkfR-gv5AOIA0TWI_do4366v6-3ZSx5r1e-r7M-Psk130_provenance
a
np:Provenance
.
dgn-np:NP292118.RAcUkfR-gv5AOIA0TWI_do4366v6-3ZSx5r1e-r7M-Psk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP292118.RAcUkfR-gv5AOIA0TWI_do4366v6-3ZSx5r1e-r7M-Psk130_assertion
{
miriam-gene:1577
a
ncit:C16612
.
lld:C0038454
a
ncit:C7057
.
dgn-gda:DGNd47ed6099b5acaa30c6501dba773aad5
sio:SIO_000628
miriam-gene:1577
,
lld:C0038454
;
a
sio:SIO_001121
.
}
dgn-np:NP292118.RAcUkfR-gv5AOIA0TWI_do4366v6-3ZSx5r1e-r7M-Psk130_provenance
{
dgn-np:NP292118.RAcUkfR-gv5AOIA0TWI_do4366v6-3ZSx5r1e-r7M-Psk130_assertion
dcterms:description
"[We then assessed the relation of allelic variants of genes modulating clopidogrel absorption (ABCB1), metabolic activation (CYP3A5 and CYP2C19), and biologic activity (P2RY12 and ITGB3) to the risk of death from any cause, nonfatal stroke, or myocardial infarction during 1 year of follow-up.]. 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:19106083
;
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:NP292118.RAcUkfR-gv5AOIA0TWI_do4366v6-3ZSx5r1e-r7M-Psk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:46+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" .
}