@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP548877.RAnN8UMq0UzWT6NkeN-0oU1aisZBZMUJt54Bt3SUQVCas
> .
@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:NP548877.RAnN8UMq0UzWT6NkeN-0oU1aisZBZMUJt54Bt3SUQVCas130_head
{
this:
np:hasAssertion
dgn-np:NP548877.RAnN8UMq0UzWT6NkeN-0oU1aisZBZMUJt54Bt3SUQVCas130_assertion
;
np:hasProvenance
dgn-np:NP548877.RAnN8UMq0UzWT6NkeN-0oU1aisZBZMUJt54Bt3SUQVCas130_provenance
;
np:hasPublicationInfo
dgn-np:NP548877.RAnN8UMq0UzWT6NkeN-0oU1aisZBZMUJt54Bt3SUQVCas130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP548877.RAnN8UMq0UzWT6NkeN-0oU1aisZBZMUJt54Bt3SUQVCas130_assertion
a
np:Assertion
.
dgn-np:NP548877.RAnN8UMq0UzWT6NkeN-0oU1aisZBZMUJt54Bt3SUQVCas130_provenance
a
np:Provenance
.
dgn-np:NP548877.RAnN8UMq0UzWT6NkeN-0oU1aisZBZMUJt54Bt3SUQVCas130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP548877.RAnN8UMq0UzWT6NkeN-0oU1aisZBZMUJt54Bt3SUQVCas130_assertion
{
miriam-gene:23771
a
ncit:C16612
.
lld:C0020456
a
ncit:C7057
.
dgn-gda:DGN1db3cd2703b48b15ff6b480ab4953f7d
sio:SIO_000628
miriam-gene:23771
,
lld:C0020456
;
a
sio:SIO_001121
.
}
dgn-np:NP548877.RAnN8UMq0UzWT6NkeN-0oU1aisZBZMUJt54Bt3SUQVCas130_provenance
{
dgn-np:NP548877.RAnN8UMq0UzWT6NkeN-0oU1aisZBZMUJt54Bt3SUQVCas130_assertion
dcterms:description
"[The insertion/deletion (I/D) polymorphism of the angiotensin I-converting enzyme (ACE) gene can modulate risk of nephropathy due to hyperglycemia, and the II genotype (producing low plasma ACE concentrations and probably reduced renal angiotensin II generation and kinin inactivation) may protect against diabetic nephropathy.]. 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:10082486
;
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:NP548877.RAnN8UMq0UzWT6NkeN-0oU1aisZBZMUJt54Bt3SUQVCas130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:31+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" .
}