@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP92681.RATm7II5K9Yifts0owLoEo40mQXetpaYj9mEzHFYtSp7o
> .
@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:NP92681.RATm7II5K9Yifts0owLoEo40mQXetpaYj9mEzHFYtSp7o130_head
{
this:
np:hasAssertion
dgn-np:NP92681.RATm7II5K9Yifts0owLoEo40mQXetpaYj9mEzHFYtSp7o130_assertion
;
np:hasProvenance
dgn-np:NP92681.RATm7II5K9Yifts0owLoEo40mQXetpaYj9mEzHFYtSp7o130_provenance
;
np:hasPublicationInfo
dgn-np:NP92681.RATm7II5K9Yifts0owLoEo40mQXetpaYj9mEzHFYtSp7o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP92681.RATm7II5K9Yifts0owLoEo40mQXetpaYj9mEzHFYtSp7o130_assertion
a
np:Assertion
.
dgn-np:NP92681.RATm7II5K9Yifts0owLoEo40mQXetpaYj9mEzHFYtSp7o130_provenance
a
np:Provenance
.
dgn-np:NP92681.RATm7II5K9Yifts0owLoEo40mQXetpaYj9mEzHFYtSp7o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP92681.RATm7II5K9Yifts0owLoEo40mQXetpaYj9mEzHFYtSp7o130_assertion
{
miriam-gene:1071
a
ncit:C16612
.
lld:C0242231
a
ncit:C7057
.
dgn-gda:DGN8cba3e45202062272c0849a5ae203835
sio:SIO_000628
miriam-gene:1071
,
lld:C0242231
;
a
sio:SIO_001122
.
}
dgn-np:NP92681.RATm7II5K9Yifts0owLoEo40mQXetpaYj9mEzHFYtSp7o130_provenance
{
dgn-np:NP92681.RATm7II5K9Yifts0owLoEo40mQXetpaYj9mEzHFYtSp7o130_assertion
dcterms:description
"[The goal of the current investigation was to determine any association between CETP polymorphisms (I405V and TaqIB), and severity of coronary stenosis, since the extent of coronary artery narrowing has been considered as a primary determinant of survival in CHD patients.]. 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:16553359
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP92681.RATm7II5K9Yifts0owLoEo40mQXetpaYj9mEzHFYtSp7o130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:46+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" .
}