@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1010156.RAXu_HnDFfl2XaTl62YNBCgmPoQCeWfRlXXU0zktp4nLc
> .
@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 dcterms: <
http://purl.org/dc/terms/
> .
@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/v4.0.0/void/
> .
dgn-np:NP1010156.RAXu_HnDFfl2XaTl62YNBCgmPoQCeWfRlXXU0zktp4nLc130_head
{
this:
np:hasAssertion
dgn-np:NP1010156.RAXu_HnDFfl2XaTl62YNBCgmPoQCeWfRlXXU0zktp4nLc130_assertion
;
np:hasProvenance
dgn-np:NP1010156.RAXu_HnDFfl2XaTl62YNBCgmPoQCeWfRlXXU0zktp4nLc130_provenance
;
np:hasPublicationInfo
dgn-np:NP1010156.RAXu_HnDFfl2XaTl62YNBCgmPoQCeWfRlXXU0zktp4nLc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1010156.RAXu_HnDFfl2XaTl62YNBCgmPoQCeWfRlXXU0zktp4nLc130_assertion
a
np:Assertion
.
dgn-np:NP1010156.RAXu_HnDFfl2XaTl62YNBCgmPoQCeWfRlXXU0zktp4nLc130_provenance
a
np:Provenance
.
dgn-np:NP1010156.RAXu_HnDFfl2XaTl62YNBCgmPoQCeWfRlXXU0zktp4nLc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1010156.RAXu_HnDFfl2XaTl62YNBCgmPoQCeWfRlXXU0zktp4nLc130_assertion
{
miriam-gene:7369
a
ncit:C16612
.
lld:C0403447
a
ncit:C7057
.
dgn-gda:DGN0ae67be6fbbeb56a3020d8f2dec7f80e
sio:SIO_000628
miriam-gene:7369
,
lld:C0403447
;
a
sio:SIO_001122
.
}
dgn-np:NP1010156.RAXu_HnDFfl2XaTl62YNBCgmPoQCeWfRlXXU0zktp4nLc130_provenance
{
dgn-np:NP1010156.RAXu_HnDFfl2XaTl62YNBCgmPoQCeWfRlXXU0zktp4nLc130_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-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1010156.RAXu_HnDFfl2XaTl62YNBCgmPoQCeWfRlXXU0zktp4nLc130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:23+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
<
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}