@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP327049.RACDt-CvsdQ126htoEfS5XxUP-IeBD1qHmsY8ySaPt-mk
> .
@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:NP327049.RACDt-CvsdQ126htoEfS5XxUP-IeBD1qHmsY8ySaPt-mk130_head
{
this:
np:hasAssertion
dgn-np:NP327049.RACDt-CvsdQ126htoEfS5XxUP-IeBD1qHmsY8ySaPt-mk130_assertion
;
np:hasProvenance
dgn-np:NP327049.RACDt-CvsdQ126htoEfS5XxUP-IeBD1qHmsY8ySaPt-mk130_provenance
;
np:hasPublicationInfo
dgn-np:NP327049.RACDt-CvsdQ126htoEfS5XxUP-IeBD1qHmsY8ySaPt-mk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP327049.RACDt-CvsdQ126htoEfS5XxUP-IeBD1qHmsY8ySaPt-mk130_assertion
a
np:Assertion
.
dgn-np:NP327049.RACDt-CvsdQ126htoEfS5XxUP-IeBD1qHmsY8ySaPt-mk130_provenance
a
np:Provenance
.
dgn-np:NP327049.RACDt-CvsdQ126htoEfS5XxUP-IeBD1qHmsY8ySaPt-mk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP327049.RACDt-CvsdQ126htoEfS5XxUP-IeBD1qHmsY8ySaPt-mk130_assertion
{
miriam-gene:183
a
ncit:C16612
.
lld:C2733225
a
ncit:C7057
.
dgn-gda:DGN6d3a49ee3d04701da0758235010c5d66
sio:SIO_000628
miriam-gene:183
,
lld:C2733225
;
a
sio:SIO_001121
.
}
dgn-np:NP327049.RACDt-CvsdQ126htoEfS5XxUP-IeBD1qHmsY8ySaPt-mk130_provenance
{
dgn-np:NP327049.RACDt-CvsdQ126htoEfS5XxUP-IeBD1qHmsY8ySaPt-mk130_assertion
dcterms:description
"[To explore the role of the angiotensinogen (AGT) gene in coronary atherosclerosis and thrombosis, we studied the effect of the AGT M235T gene variant on plasma AGT levels and BP in patients with coronary artery disease and in the subgroup of survivors of myocardial infarction as compared with angiographically defined control subjects.]. 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:10097233
;
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:NP327049.RACDt-CvsdQ126htoEfS5XxUP-IeBD1qHmsY8ySaPt-mk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:11+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" .
}