@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP426628.RAVvEv4PEkaL5lFNYMQfE0QfBU6MlZpFHXlBGfJvy1_a0
> .
@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:NP426628.RAVvEv4PEkaL5lFNYMQfE0QfBU6MlZpFHXlBGfJvy1_a0130_assertion
;
np:hasProvenance
dgn-np:NP426628.RAVvEv4PEkaL5lFNYMQfE0QfBU6MlZpFHXlBGfJvy1_a0130_provenance
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np:hasPublicationInfo
dgn-np:NP426628.RAVvEv4PEkaL5lFNYMQfE0QfBU6MlZpFHXlBGfJvy1_a0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP426628.RAVvEv4PEkaL5lFNYMQfE0QfBU6MlZpFHXlBGfJvy1_a0130_assertion
a
np:Assertion
.
dgn-np:NP426628.RAVvEv4PEkaL5lFNYMQfE0QfBU6MlZpFHXlBGfJvy1_a0130_provenance
a
np:Provenance
.
dgn-np:NP426628.RAVvEv4PEkaL5lFNYMQfE0QfBU6MlZpFHXlBGfJvy1_a0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP426628.RAVvEv4PEkaL5lFNYMQfE0QfBU6MlZpFHXlBGfJvy1_a0130_assertion
{
miriam-gene:7369
a
ncit:C16612
.
lld:C1561643
a
ncit:C7057
.
dgn-gda:DGNe1d7f289aa3be729d9f7a9d906ec7020
sio:SIO_000628
miriam-gene:7369
,
lld:C1561643
;
a
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.
}
dgn-np:NP426628.RAVvEv4PEkaL5lFNYMQfE0QfBU6MlZpFHXlBGfJvy1_a0130_provenance
{
dgn-np:NP426628.RAVvEv4PEkaL5lFNYMQfE0QfBU6MlZpFHXlBGfJvy1_a0130_assertion
dcterms:description
"[We report mutation analysis of the REN gene in 39 kindreds with hyperuricemia and CKD who previously tested negative for mutations in the UMOD (uromodulin) and HNF1B (hepatocyte nuclear factor 1β) genes.]. 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:21903317
;
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:NP426628.RAVvEv4PEkaL5lFNYMQfE0QfBU6MlZpFHXlBGfJvy1_a0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:13+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
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dgn-void:disgenetrdf
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"v2.1.0" .
}