@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP884519.RAwD8kJNaSouVmvJ4wOZbou3AVsycz22TakRhk_IxUlMI
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP884519.RAwD8kJNaSouVmvJ4wOZbou3AVsycz22TakRhk_IxUlMI130_assertion
;
np:hasProvenance
dgn-np:NP884519.RAwD8kJNaSouVmvJ4wOZbou3AVsycz22TakRhk_IxUlMI130_provenance
;
np:hasPublicationInfo
dgn-np:NP884519.RAwD8kJNaSouVmvJ4wOZbou3AVsycz22TakRhk_IxUlMI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP884519.RAwD8kJNaSouVmvJ4wOZbou3AVsycz22TakRhk_IxUlMI130_assertion
a
np:Assertion
.
dgn-np:NP884519.RAwD8kJNaSouVmvJ4wOZbou3AVsycz22TakRhk_IxUlMI130_provenance
a
np:Provenance
.
dgn-np:NP884519.RAwD8kJNaSouVmvJ4wOZbou3AVsycz22TakRhk_IxUlMI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP884519.RAwD8kJNaSouVmvJ4wOZbou3AVsycz22TakRhk_IxUlMI130_assertion
{
miriam-gene:7369
a
ncit:C16612
.
lld:C0403447
a
ncit:C7057
.
dgn-gda:DGN41f34f5d25df07a6dac7337a305f816f
sio:SIO_000628
miriam-gene:7369
,
lld:C0403447
;
a
sio:SIO_001121
.
}
dgn-np:NP884519.RAwD8kJNaSouVmvJ4wOZbou3AVsycz22TakRhk_IxUlMI130_provenance
{
dgn-np:NP884519.RAwD8kJNaSouVmvJ4wOZbou3AVsycz22TakRhk_IxUlMI130_assertion
dcterms:description
"[In recent genetic association studies, common variants including rs12917707 in the UMOD locus have shown strong evidence of association with eGFR, prevalent and incident chronic kidney disease and uromodulin urinary concentration in general population cohorts.]. 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:22947327
;
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:NP884519.RAwD8kJNaSouVmvJ4wOZbou3AVsycz22TakRhk_IxUlMI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:00+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" .
}