@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1409775.RAURrkTnQD8G38J4R2iafMeU8SYUxcz-kj5-EMwB_AdTQ
> .
@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:NP1409775.RAURrkTnQD8G38J4R2iafMeU8SYUxcz-kj5-EMwB_AdTQ130_head
{
this:
np:hasAssertion
dgn-np:NP1409775.RAURrkTnQD8G38J4R2iafMeU8SYUxcz-kj5-EMwB_AdTQ130_assertion
;
np:hasProvenance
dgn-np:NP1409775.RAURrkTnQD8G38J4R2iafMeU8SYUxcz-kj5-EMwB_AdTQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP1409775.RAURrkTnQD8G38J4R2iafMeU8SYUxcz-kj5-EMwB_AdTQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1409775.RAURrkTnQD8G38J4R2iafMeU8SYUxcz-kj5-EMwB_AdTQ130_assertion
a
np:Assertion
.
dgn-np:NP1409775.RAURrkTnQD8G38J4R2iafMeU8SYUxcz-kj5-EMwB_AdTQ130_provenance
a
np:Provenance
.
dgn-np:NP1409775.RAURrkTnQD8G38J4R2iafMeU8SYUxcz-kj5-EMwB_AdTQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1409775.RAURrkTnQD8G38J4R2iafMeU8SYUxcz-kj5-EMwB_AdTQ130_assertion
{
miriam-gene:183
a
ncit:C16612
.
lld:C0085580
a
ncit:C7057
.
dgn-gda:DGNfd993d3e0b7cfd1bc3113b3f4458c053
sio:SIO_000628
miriam-gene:183
,
lld:C0085580
;
a
sio:SIO_001121
.
}
dgn-np:NP1409775.RAURrkTnQD8G38J4R2iafMeU8SYUxcz-kj5-EMwB_AdTQ130_provenance
{
dgn-np:NP1409775.RAURrkTnQD8G38J4R2iafMeU8SYUxcz-kj5-EMwB_AdTQ130_assertion
dcterms:description
"[To date, the human angiotensinogen (AGT) gene and some of its variants represent the best examples of genetic influences that are involved in the determination of essential hypertension (EH) and associated cardiovascular diseases (CVDs).]. 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:9831339
;
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:NP1409775.RAURrkTnQD8G38J4R2iafMeU8SYUxcz-kj5-EMwB_AdTQ130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:52:25+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" .
}