@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1321692.RAGCAue7mSlaccS1hAqowCgAieOm_L0Zuy89-waW0D1wk
> .
@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:NP1321692.RAGCAue7mSlaccS1hAqowCgAieOm_L0Zuy89-waW0D1wk130_head
{
this:
np:hasAssertion
dgn-np:NP1321692.RAGCAue7mSlaccS1hAqowCgAieOm_L0Zuy89-waW0D1wk130_assertion
;
np:hasProvenance
dgn-np:NP1321692.RAGCAue7mSlaccS1hAqowCgAieOm_L0Zuy89-waW0D1wk130_provenance
;
np:hasPublicationInfo
dgn-np:NP1321692.RAGCAue7mSlaccS1hAqowCgAieOm_L0Zuy89-waW0D1wk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1321692.RAGCAue7mSlaccS1hAqowCgAieOm_L0Zuy89-waW0D1wk130_assertion
a
np:Assertion
.
dgn-np:NP1321692.RAGCAue7mSlaccS1hAqowCgAieOm_L0Zuy89-waW0D1wk130_provenance
a
np:Provenance
.
dgn-np:NP1321692.RAGCAue7mSlaccS1hAqowCgAieOm_L0Zuy89-waW0D1wk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1321692.RAGCAue7mSlaccS1hAqowCgAieOm_L0Zuy89-waW0D1wk130_assertion
{
miriam-gene:183
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGNa48dd03336716f5ca38835a5c014bd4a
sio:SIO_000628
miriam-gene:183
,
lld:C0020538
;
a
sio:SIO_001121
.
}
dgn-np:NP1321692.RAGCAue7mSlaccS1hAqowCgAieOm_L0Zuy89-waW0D1wk130_provenance
{
dgn-np:NP1321692.RAGCAue7mSlaccS1hAqowCgAieOm_L0Zuy89-waW0D1wk130_assertion
dcterms:description
"[There have been reports linking a homozygous deletion allele of the angiotensin converting enzyme (ACE) gene (DD) with an increased risk of myocardial infarction, and some variants of the angiotensinogen gene with an increased risk of hypertension.]. 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:7783537
;
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:NP1321692.RAGCAue7mSlaccS1hAqowCgAieOm_L0Zuy89-waW0D1wk130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:45+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" .
}