@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP224953.RAgkwu0dscubOf4CF-2F26r38IwEOiMxh9QP4i34vuQ3Y
> .
@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:NP224953.RAgkwu0dscubOf4CF-2F26r38IwEOiMxh9QP4i34vuQ3Y130_head
{
this:
np:hasAssertion
dgn-np:NP224953.RAgkwu0dscubOf4CF-2F26r38IwEOiMxh9QP4i34vuQ3Y130_assertion
;
np:hasProvenance
dgn-np:NP224953.RAgkwu0dscubOf4CF-2F26r38IwEOiMxh9QP4i34vuQ3Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP224953.RAgkwu0dscubOf4CF-2F26r38IwEOiMxh9QP4i34vuQ3Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP224953.RAgkwu0dscubOf4CF-2F26r38IwEOiMxh9QP4i34vuQ3Y130_assertion
a
np:Assertion
.
dgn-np:NP224953.RAgkwu0dscubOf4CF-2F26r38IwEOiMxh9QP4i34vuQ3Y130_provenance
a
np:Provenance
.
dgn-np:NP224953.RAgkwu0dscubOf4CF-2F26r38IwEOiMxh9QP4i34vuQ3Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP224953.RAgkwu0dscubOf4CF-2F26r38IwEOiMxh9QP4i34vuQ3Y130_assertion
{
miriam-gene:1636
a
ncit:C16612
.
lld:C0035309
a
ncit:C7057
.
dgn-gda:DGNde40464c60eb7cc033cbd39db5146370
sio:SIO_000628
miriam-gene:1636
,
lld:C0035309
;
a
sio:SIO_001121
.
}
dgn-np:NP224953.RAgkwu0dscubOf4CF-2F26r38IwEOiMxh9QP4i34vuQ3Y130_provenance
{
dgn-np:NP224953.RAgkwu0dscubOf4CF-2F26r38IwEOiMxh9QP4i34vuQ3Y130_assertion
dcterms:description
"[In conclusion, the D allele of the ACE gene is associated with microalbuminuria as well as with retinopathy and left ventricular hypertrophy, and seems to be an independent risk factor for target organ damage in essential 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:8989733
;
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:NP224953.RAgkwu0dscubOf4CF-2F26r38IwEOiMxh9QP4i34vuQ3Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:05+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" .
}