@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1224494.RAVTRIDdW7Bz10b-Uz9jz0na5Jy1M0Zd_GWxslZ4ZSmyA
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1224494.RAVTRIDdW7Bz10b-Uz9jz0na5Jy1M0Zd_GWxslZ4ZSmyA130_head
{
this:
np:hasAssertion
dgn-np:NP1224494.RAVTRIDdW7Bz10b-Uz9jz0na5Jy1M0Zd_GWxslZ4ZSmyA130_assertion
;
np:hasProvenance
dgn-np:NP1224494.RAVTRIDdW7Bz10b-Uz9jz0na5Jy1M0Zd_GWxslZ4ZSmyA130_provenance
;
np:hasPublicationInfo
dgn-np:NP1224494.RAVTRIDdW7Bz10b-Uz9jz0na5Jy1M0Zd_GWxslZ4ZSmyA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1224494.RAVTRIDdW7Bz10b-Uz9jz0na5Jy1M0Zd_GWxslZ4ZSmyA130_assertion
a
np:Assertion
.
dgn-np:NP1224494.RAVTRIDdW7Bz10b-Uz9jz0na5Jy1M0Zd_GWxslZ4ZSmyA130_provenance
a
np:Provenance
.
dgn-np:NP1224494.RAVTRIDdW7Bz10b-Uz9jz0na5Jy1M0Zd_GWxslZ4ZSmyA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1224494.RAVTRIDdW7Bz10b-Uz9jz0na5Jy1M0Zd_GWxslZ4ZSmyA130_assertion
{
miriam-gene:1557
a
ncit:C16612
.
lld:C1561643
a
ncit:C7057
.
dgn-gda:DGNef3ae633299fc15c2a907b7b2e630647
sio:SIO_000628
miriam-gene:1557
,
lld:C1561643
;
a
sio:SIO_001121
.
}
dgn-np:NP1224494.RAVTRIDdW7Bz10b-Uz9jz0na5Jy1M0Zd_GWxslZ4ZSmyA130_provenance
{
dgn-np:NP1224494.RAVTRIDdW7Bz10b-Uz9jz0na5Jy1M0Zd_GWxslZ4ZSmyA130_assertion
dcterms:description
"[We analyzed the incidence of CYP2C19 polymorphism and its association with the development of CAD in the absence of diabetes, dyslipidemia, and chronic kidney disease to minimize the influence of conventional coronary risk factors.]. 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:25264752
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1224494.RAVTRIDdW7Bz10b-Uz9jz0na5Jy1M0Zd_GWxslZ4ZSmyA130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:01+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}