@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP367485.RAiMHKMvTlBwwECMzjET92Xnf-tjyxeNkNq-cOi03kADY
> .
@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:NP367485.RAiMHKMvTlBwwECMzjET92Xnf-tjyxeNkNq-cOi03kADY130_head
{
this:
np:hasAssertion
dgn-np:NP367485.RAiMHKMvTlBwwECMzjET92Xnf-tjyxeNkNq-cOi03kADY130_assertion
;
np:hasProvenance
dgn-np:NP367485.RAiMHKMvTlBwwECMzjET92Xnf-tjyxeNkNq-cOi03kADY130_provenance
;
np:hasPublicationInfo
dgn-np:NP367485.RAiMHKMvTlBwwECMzjET92Xnf-tjyxeNkNq-cOi03kADY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP367485.RAiMHKMvTlBwwECMzjET92Xnf-tjyxeNkNq-cOi03kADY130_assertion
a
np:Assertion
.
dgn-np:NP367485.RAiMHKMvTlBwwECMzjET92Xnf-tjyxeNkNq-cOi03kADY130_provenance
a
np:Provenance
.
dgn-np:NP367485.RAiMHKMvTlBwwECMzjET92Xnf-tjyxeNkNq-cOi03kADY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP367485.RAiMHKMvTlBwwECMzjET92Xnf-tjyxeNkNq-cOi03kADY130_assertion
{
miriam-gene:1576
a
ncit:C16612
.
lld:C0948089
a
ncit:C7057
.
dgn-gda:DGN728a70288b357dc134ba171b3bd03c9f
sio:SIO_000628
miriam-gene:1576
,
lld:C0948089
;
a
sio:SIO_001121
.
}
dgn-np:NP367485.RAiMHKMvTlBwwECMzjET92Xnf-tjyxeNkNq-cOi03kADY130_provenance
{
dgn-np:NP367485.RAiMHKMvTlBwwECMzjET92Xnf-tjyxeNkNq-cOi03kADY130_assertion
dcterms:description
"[This research evaluated the frequency of variant alleles in the genes coding for CYP3A4, CYP3A5, CYP2C9, and CYP2C19 enzymes in patients on clopidogrel therapy and experiencing repeat acute coronary syndrome (ACS) compared to a control group with a matching ethnic composition.]. 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:19337788
;
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:NP367485.RAiMHKMvTlBwwECMzjET92Xnf-tjyxeNkNq-cOi03kADY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:35+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" .
}