@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP221560.RAWvQtRBzBYUNTg3-dX8mmy8Lbqg2ji5IkN3TGrqlLKIM
> .
@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:NP221560.RAWvQtRBzBYUNTg3-dX8mmy8Lbqg2ji5IkN3TGrqlLKIM130_head
{
this:
np:hasAssertion
dgn-np:NP221560.RAWvQtRBzBYUNTg3-dX8mmy8Lbqg2ji5IkN3TGrqlLKIM130_assertion
;
np:hasProvenance
dgn-np:NP221560.RAWvQtRBzBYUNTg3-dX8mmy8Lbqg2ji5IkN3TGrqlLKIM130_provenance
;
np:hasPublicationInfo
dgn-np:NP221560.RAWvQtRBzBYUNTg3-dX8mmy8Lbqg2ji5IkN3TGrqlLKIM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP221560.RAWvQtRBzBYUNTg3-dX8mmy8Lbqg2ji5IkN3TGrqlLKIM130_assertion
a
np:Assertion
.
dgn-np:NP221560.RAWvQtRBzBYUNTg3-dX8mmy8Lbqg2ji5IkN3TGrqlLKIM130_provenance
a
np:Provenance
.
dgn-np:NP221560.RAWvQtRBzBYUNTg3-dX8mmy8Lbqg2ji5IkN3TGrqlLKIM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP221560.RAWvQtRBzBYUNTg3-dX8mmy8Lbqg2ji5IkN3TGrqlLKIM130_assertion
{
miriam-gene:9360
a
ncit:C16612
.
lld:C0038454
a
ncit:C7057
.
dgn-gda:DGN185c425462983b8105469fd7e8ed68c1
sio:SIO_000628
miriam-gene:9360
,
lld:C0038454
;
a
sio:SIO_001121
.
}
dgn-np:NP221560.RAWvQtRBzBYUNTg3-dX8mmy8Lbqg2ji5IkN3TGrqlLKIM130_provenance
{
dgn-np:NP221560.RAWvQtRBzBYUNTg3-dX8mmy8Lbqg2ji5IkN3TGrqlLKIM130_assertion
dcterms:description
"[Consistent with these findings, in subjects with acute coronary syndromes treated with prasugrel, no significant associations were found between any of the tested CYP genotypes and risk of cardiovascular death, myocardial infarction, or stroke.]. 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:19414633
;
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:NP221560.RAWvQtRBzBYUNTg3-dX8mmy8Lbqg2ji5IkN3TGrqlLKIM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:03+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" .
}