@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP772.RA6sYWzWALmZ_DckZ72NRZ0cJOFOTY_WU6T4KM75p0j3k
> .
@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 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/v3.0.0/void/
> .
dgn-np:NP772.RA6sYWzWALmZ_DckZ72NRZ0cJOFOTY_WU6T4KM75p0j3k130_head
{
this:
np:hasAssertion
dgn-np:NP772.RA6sYWzWALmZ_DckZ72NRZ0cJOFOTY_WU6T4KM75p0j3k130_assertion
;
np:hasProvenance
dgn-np:NP772.RA6sYWzWALmZ_DckZ72NRZ0cJOFOTY_WU6T4KM75p0j3k130_provenance
;
np:hasPublicationInfo
dgn-np:NP772.RA6sYWzWALmZ_DckZ72NRZ0cJOFOTY_WU6T4KM75p0j3k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP772.RA6sYWzWALmZ_DckZ72NRZ0cJOFOTY_WU6T4KM75p0j3k130_assertion
a
np:Assertion
.
dgn-np:NP772.RA6sYWzWALmZ_DckZ72NRZ0cJOFOTY_WU6T4KM75p0j3k130_provenance
a
np:Provenance
.
dgn-np:NP772.RA6sYWzWALmZ_DckZ72NRZ0cJOFOTY_WU6T4KM75p0j3k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP772.RA6sYWzWALmZ_DckZ72NRZ0cJOFOTY_WU6T4KM75p0j3k130_assertion
{
miriam-gene:183
a
ncit:C16612
.
lld:C0266313
a
ncit:C7057
.
dgn-gda:DGN8f323adb8c96c6d6c828332a48c58f26
sio:SIO_000628
miriam-gene:183
,
lld:C0266313
;
a
sio:SIO_001122
.
}
dgn-np:NP772.RA6sYWzWALmZ_DckZ72NRZ0cJOFOTY_WU6T4KM75p0j3k130_provenance
{
dgn-np:NP772.RA6sYWzWALmZ_DckZ72NRZ0cJOFOTY_WU6T4KM75p0j3k130_assertion
dcterms:description
"[We studied 11 individuals with renal tubular dysgenesis, belonging to nine families, and found that they had homozygous or compound heterozygous mutations in the genes encoding renin, angiotensinogen, angiotensin converting enzyme or angiotensin II receptor type 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_curated
;
sio:SIO_000772
miriam-pubmed:16116425
;
prov:wasDerivedFrom
dgn-void:uniprot-20150221
;
prov:wasGeneratedBy
eco:ECO_0000218
.
dgn-void:source_evidence_curated
a
eco:ECO_0000205
;
rdfs:comment
"Gene-disease associations manually curated."@en ;
rdfs:label
"DisGeNET evidence - CURATED"@en .
dgn-void:uniprot-20150221
pav:importedOn
"2015-02-21"^^
xsd:date
.
}
dgn-np:NP772.RA6sYWzWALmZ_DckZ72NRZ0cJOFOTY_WU6T4KM75p0j3k130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:37:42+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
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}