@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP759119.RAMdjKzvhvH3T4EvPnBDTbxOeYdT_TGV3wbP7QTShZqS0
> .
@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:NP759119.RAMdjKzvhvH3T4EvPnBDTbxOeYdT_TGV3wbP7QTShZqS0130_head
{
this:
np:hasAssertion
dgn-np:NP759119.RAMdjKzvhvH3T4EvPnBDTbxOeYdT_TGV3wbP7QTShZqS0130_assertion
;
np:hasProvenance
dgn-np:NP759119.RAMdjKzvhvH3T4EvPnBDTbxOeYdT_TGV3wbP7QTShZqS0130_provenance
;
np:hasPublicationInfo
dgn-np:NP759119.RAMdjKzvhvH3T4EvPnBDTbxOeYdT_TGV3wbP7QTShZqS0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP759119.RAMdjKzvhvH3T4EvPnBDTbxOeYdT_TGV3wbP7QTShZqS0130_assertion
a
np:Assertion
.
dgn-np:NP759119.RAMdjKzvhvH3T4EvPnBDTbxOeYdT_TGV3wbP7QTShZqS0130_provenance
a
np:Provenance
.
dgn-np:NP759119.RAMdjKzvhvH3T4EvPnBDTbxOeYdT_TGV3wbP7QTShZqS0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP759119.RAMdjKzvhvH3T4EvPnBDTbxOeYdT_TGV3wbP7QTShZqS0130_assertion
{
miriam-gene:1636
a
ncit:C16612
.
lld:C0242231
a
ncit:C7057
.
dgn-gda:DGN05a121fb006a3b76a3880403b2606fcf
sio:SIO_000628
miriam-gene:1636
,
lld:C0242231
;
a
sio:SIO_001121
.
}
dgn-np:NP759119.RAMdjKzvhvH3T4EvPnBDTbxOeYdT_TGV3wbP7QTShZqS0130_provenance
{
dgn-np:NP759119.RAMdjKzvhvH3T4EvPnBDTbxOeYdT_TGV3wbP7QTShZqS0130_assertion
dcterms:description
"[To explore the relation of angiotensin-converting enzyme (ACE) and angiotensin II type 1 receptor (AT1R) gene polymorphism with coronary heart disease (CHD) and the severity of coronary artery stenosis, 130 CHD patients who underwent coronary angiography were examined for the number of affected coronary vessels (> or = 75% stenosis) and coronary Jeopardy score.]. 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:18231736
;
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:NP759119.RAMdjKzvhvH3T4EvPnBDTbxOeYdT_TGV3wbP7QTShZqS0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:39+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" .
}