@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP577434.RATv_f-E5wtbF6gyqESBQs3h0Ds1geHqhQXNo7ayOVElI
> .
@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:NP577434.RATv_f-E5wtbF6gyqESBQs3h0Ds1geHqhQXNo7ayOVElI130_head
{
this:
np:hasAssertion
dgn-np:NP577434.RATv_f-E5wtbF6gyqESBQs3h0Ds1geHqhQXNo7ayOVElI130_assertion
;
np:hasProvenance
dgn-np:NP577434.RATv_f-E5wtbF6gyqESBQs3h0Ds1geHqhQXNo7ayOVElI130_provenance
;
np:hasPublicationInfo
dgn-np:NP577434.RATv_f-E5wtbF6gyqESBQs3h0Ds1geHqhQXNo7ayOVElI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP577434.RATv_f-E5wtbF6gyqESBQs3h0Ds1geHqhQXNo7ayOVElI130_assertion
a
np:Assertion
.
dgn-np:NP577434.RATv_f-E5wtbF6gyqESBQs3h0Ds1geHqhQXNo7ayOVElI130_provenance
a
np:Provenance
.
dgn-np:NP577434.RATv_f-E5wtbF6gyqESBQs3h0Ds1geHqhQXNo7ayOVElI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP577434.RATv_f-E5wtbF6gyqESBQs3h0Ds1geHqhQXNo7ayOVElI130_assertion
{
miriam-gene:23771
a
ncit:C16612
.
lld:C0022658
a
ncit:C7057
.
dgn-gda:DGNd3330eb707c70696a0ce705f98bdb200
sio:SIO_000628
miriam-gene:23771
,
lld:C0022658
;
a
sio:SIO_001121
.
}
dgn-np:NP577434.RATv_f-E5wtbF6gyqESBQs3h0Ds1geHqhQXNo7ayOVElI130_provenance
{
dgn-np:NP577434.RATv_f-E5wtbF6gyqESBQs3h0Ds1geHqhQXNo7ayOVElI130_assertion
dcterms:description
"[Although genes have not been definitely linked to renal vascular disease, population- and family-based epidemiology of kidney disease, segregation analysis of Pima and Caucasian families in which diabetic nephropathy is clustered, and the positional cloning of genes responsible for rare, familial glomerulosclerosis syndromes support the hypothesis that genes regulate the pathogenesis of renal disease.]. 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:12496669
;
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:NP577434.RATv_f-E5wtbF6gyqESBQs3h0Ds1geHqhQXNo7ayOVElI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:48+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" .
}