@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP280288.RA3Pq71xMsk1BKldFJqnFx35HxhMKa1sray2ldabqC8-M
> .
@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:NP280288.RA3Pq71xMsk1BKldFJqnFx35HxhMKa1sray2ldabqC8-M130_head
{
this:
np:hasAssertion
dgn-np:NP280288.RA3Pq71xMsk1BKldFJqnFx35HxhMKa1sray2ldabqC8-M130_assertion
;
np:hasProvenance
dgn-np:NP280288.RA3Pq71xMsk1BKldFJqnFx35HxhMKa1sray2ldabqC8-M130_provenance
;
np:hasPublicationInfo
dgn-np:NP280288.RA3Pq71xMsk1BKldFJqnFx35HxhMKa1sray2ldabqC8-M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP280288.RA3Pq71xMsk1BKldFJqnFx35HxhMKa1sray2ldabqC8-M130_assertion
a
np:Assertion
.
dgn-np:NP280288.RA3Pq71xMsk1BKldFJqnFx35HxhMKa1sray2ldabqC8-M130_provenance
a
np:Provenance
.
dgn-np:NP280288.RA3Pq71xMsk1BKldFJqnFx35HxhMKa1sray2ldabqC8-M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP280288.RA3Pq71xMsk1BKldFJqnFx35HxhMKa1sray2ldabqC8-M130_assertion
{
miriam-gene:1636
a
ncit:C16612
.
lld:C0017661
a
ncit:C7057
.
dgn-gda:DGN8b6274123d152887f9a80b759999a14e
sio:SIO_000628
miriam-gene:1636
,
lld:C0017661
;
a
sio:SIO_001121
.
}
dgn-np:NP280288.RA3Pq71xMsk1BKldFJqnFx35HxhMKa1sray2ldabqC8-M130_provenance
{
dgn-np:NP280288.RA3Pq71xMsk1BKldFJqnFx35HxhMKa1sray2ldabqC8-M130_assertion
dcterms:description
"[Individuals with IgA nephropathy (IgAN) who are homozygous for the deletion (D) polymorphism of the gene for angiotensin converting enzyme (ACE) are reported to be at increased risk of progressive renal damage.]. 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:10752761
;
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:NP280288.RA3Pq71xMsk1BKldFJqnFx35HxhMKa1sray2ldabqC8-M130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:43:52+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" .
}