@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP411916.RAEXoB4DrR_deuGHs3Q8t4qfrY2ZTIEspyvYHuXoUV7CU
> .
@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:NP411916.RAEXoB4DrR_deuGHs3Q8t4qfrY2ZTIEspyvYHuXoUV7CU130_head
{
this:
np:hasAssertion
dgn-np:NP411916.RAEXoB4DrR_deuGHs3Q8t4qfrY2ZTIEspyvYHuXoUV7CU130_assertion
;
np:hasProvenance
dgn-np:NP411916.RAEXoB4DrR_deuGHs3Q8t4qfrY2ZTIEspyvYHuXoUV7CU130_provenance
;
np:hasPublicationInfo
dgn-np:NP411916.RAEXoB4DrR_deuGHs3Q8t4qfrY2ZTIEspyvYHuXoUV7CU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP411916.RAEXoB4DrR_deuGHs3Q8t4qfrY2ZTIEspyvYHuXoUV7CU130_assertion
a
np:Assertion
.
dgn-np:NP411916.RAEXoB4DrR_deuGHs3Q8t4qfrY2ZTIEspyvYHuXoUV7CU130_provenance
a
np:Provenance
.
dgn-np:NP411916.RAEXoB4DrR_deuGHs3Q8t4qfrY2ZTIEspyvYHuXoUV7CU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP411916.RAEXoB4DrR_deuGHs3Q8t4qfrY2ZTIEspyvYHuXoUV7CU130_assertion
{
miriam-gene:1636
a
ncit:C16612
.
lld:C1968949
a
ncit:C7057
.
dgn-gda:DGN5da3d4f9fd26d8703ea81bc3db1ed6ba
sio:SIO_000628
miriam-gene:1636
,
lld:C1968949
;
a
sio:SIO_001121
.
}
dgn-np:NP411916.RAEXoB4DrR_deuGHs3Q8t4qfrY2ZTIEspyvYHuXoUV7CU130_provenance
{
dgn-np:NP411916.RAEXoB4DrR_deuGHs3Q8t4qfrY2ZTIEspyvYHuXoUV7CU130_assertion
dcterms:description
"[ACE genotype distribution in children with CAKUT was no different from that of the control subjects, but the subgroup of patients with radiographic renal parenchymal abnormalities showed an increased occurrence of the D/D genotype.]. 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:15470205
;
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:NP411916.RAEXoB4DrR_deuGHs3Q8t4qfrY2ZTIEspyvYHuXoUV7CU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:04+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" .
}