@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP488640.RAYtNnowmC2IzKq22a68JtrcpAhqtYlWt2ny8BZB5AFy4
> .
@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:NP488640.RAYtNnowmC2IzKq22a68JtrcpAhqtYlWt2ny8BZB5AFy4130_head
{
this:
np:hasAssertion
dgn-np:NP488640.RAYtNnowmC2IzKq22a68JtrcpAhqtYlWt2ny8BZB5AFy4130_assertion
;
np:hasProvenance
dgn-np:NP488640.RAYtNnowmC2IzKq22a68JtrcpAhqtYlWt2ny8BZB5AFy4130_provenance
;
np:hasPublicationInfo
dgn-np:NP488640.RAYtNnowmC2IzKq22a68JtrcpAhqtYlWt2ny8BZB5AFy4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP488640.RAYtNnowmC2IzKq22a68JtrcpAhqtYlWt2ny8BZB5AFy4130_assertion
a
np:Assertion
.
dgn-np:NP488640.RAYtNnowmC2IzKq22a68JtrcpAhqtYlWt2ny8BZB5AFy4130_provenance
a
np:Provenance
.
dgn-np:NP488640.RAYtNnowmC2IzKq22a68JtrcpAhqtYlWt2ny8BZB5AFy4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP488640.RAYtNnowmC2IzKq22a68JtrcpAhqtYlWt2ny8BZB5AFy4130_assertion
{
miriam-gene:1557
a
ncit:C16612
.
lld:C0010054
a
ncit:C7057
.
dgn-gda:DGN31a80b86902dc4104d9d60d0aace5d62
sio:SIO_000628
miriam-gene:1557
,
lld:C0010054
;
a
sio:SIO_001121
.
}
dgn-np:NP488640.RAYtNnowmC2IzKq22a68JtrcpAhqtYlWt2ny8BZB5AFy4130_provenance
{
dgn-np:NP488640.RAYtNnowmC2IzKq22a68JtrcpAhqtYlWt2ny8BZB5AFy4130_assertion
dcterms:description
"[In conclusion, carrier status for LOF CYP2C19 is associated with an increased risk of adverse clinical events in patients with coronary artery disease on clopidogrel therapy despite differences in clinical significance according to ethnicity.]. 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:22591668
;
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:NP488640.RAYtNnowmC2IzKq22a68JtrcpAhqtYlWt2ny8BZB5AFy4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:52+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" .
}