@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP7934.RAOneYJzOQiqZn9aDGtDkq4Q7UeNiSYuNSfDZi6QDl95Q
> .
@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:NP7934.RAOneYJzOQiqZn9aDGtDkq4Q7UeNiSYuNSfDZi6QDl95Q130_head
{
this:
np:hasAssertion
dgn-np:NP7934.RAOneYJzOQiqZn9aDGtDkq4Q7UeNiSYuNSfDZi6QDl95Q130_assertion
;
np:hasProvenance
dgn-np:NP7934.RAOneYJzOQiqZn9aDGtDkq4Q7UeNiSYuNSfDZi6QDl95Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP7934.RAOneYJzOQiqZn9aDGtDkq4Q7UeNiSYuNSfDZi6QDl95Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP7934.RAOneYJzOQiqZn9aDGtDkq4Q7UeNiSYuNSfDZi6QDl95Q130_assertion
a
np:Assertion
.
dgn-np:NP7934.RAOneYJzOQiqZn9aDGtDkq4Q7UeNiSYuNSfDZi6QDl95Q130_provenance
a
np:Provenance
.
dgn-np:NP7934.RAOneYJzOQiqZn9aDGtDkq4Q7UeNiSYuNSfDZi6QDl95Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP7934.RAOneYJzOQiqZn9aDGtDkq4Q7UeNiSYuNSfDZi6QDl95Q130_assertion
{
miriam-gene:183
a
ncit:C16612
.
lld:C0266313
a
ncit:C7057
.
dgn-gda:DGNebfb5dc1b877db43cb461627ebf5a0b9
sio:SIO_000628
miriam-gene:183
,
lld:C0266313
;
a
sio:SIO_001121
.
}
dgn-np:NP7934.RAOneYJzOQiqZn9aDGtDkq4Q7UeNiSYuNSfDZi6QDl95Q130_provenance
{
dgn-np:NP7934.RAOneYJzOQiqZn9aDGtDkq4Q7UeNiSYuNSfDZi6QDl95Q130_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:ctd_human-20130708
;
prov:wasGeneratedBy
eco:ECO_0000218
.
dgn-void:ctd_human-20130708
pav:importedOn
"2013-07-24"^^
xsd:date
.
dgn-void:source_evidence_curated
a
eco:ECO_0000205
;
rdfs:comment
"Gene-disease associations manually curated."@en ;
rdfs:label
"DisGeNET evidence - CURATED"@en .
}
dgn-np:NP7934.RAOneYJzOQiqZn9aDGtDkq4Q7UeNiSYuNSfDZi6QDl95Q130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:01+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" .
}