@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP486970.RAyBOaUXPBTjUCdEmdFKv3cBCyK7yCCJUZlOE22hERK5A
> .
@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:NP486970.RAyBOaUXPBTjUCdEmdFKv3cBCyK7yCCJUZlOE22hERK5A130_head
{
this:
np:hasAssertion
dgn-np:NP486970.RAyBOaUXPBTjUCdEmdFKv3cBCyK7yCCJUZlOE22hERK5A130_assertion
;
np:hasProvenance
dgn-np:NP486970.RAyBOaUXPBTjUCdEmdFKv3cBCyK7yCCJUZlOE22hERK5A130_provenance
;
np:hasPublicationInfo
dgn-np:NP486970.RAyBOaUXPBTjUCdEmdFKv3cBCyK7yCCJUZlOE22hERK5A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP486970.RAyBOaUXPBTjUCdEmdFKv3cBCyK7yCCJUZlOE22hERK5A130_assertion
a
np:Assertion
.
dgn-np:NP486970.RAyBOaUXPBTjUCdEmdFKv3cBCyK7yCCJUZlOE22hERK5A130_provenance
a
np:Provenance
.
dgn-np:NP486970.RAyBOaUXPBTjUCdEmdFKv3cBCyK7yCCJUZlOE22hERK5A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP486970.RAyBOaUXPBTjUCdEmdFKv3cBCyK7yCCJUZlOE22hERK5A130_assertion
{
miriam-gene:7369
a
ncit:C16612
.
lld:C0268113
a
ncit:C7057
.
dgn-gda:DGN9bed165104b50d1f3221417222a8dd77
sio:SIO_000628
miriam-gene:7369
,
lld:C0268113
;
a
sio:SIO_001121
.
}
dgn-np:NP486970.RAyBOaUXPBTjUCdEmdFKv3cBCyK7yCCJUZlOE22hERK5A130_provenance
{
dgn-np:NP486970.RAyBOaUXPBTjUCdEmdFKv3cBCyK7yCCJUZlOE22hERK5A130_assertion
dcterms:description
"[Elucidation of the mechanisms of hyperuricemia in patients with familial juvenile hyperuricemic nephropathy will shed light on the function of uromodulin, functional impairment of which eventually results in diminished uric acid excretion.]. 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:18349750
;
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:NP486970.RAyBOaUXPBTjUCdEmdFKv3cBCyK7yCCJUZlOE22hERK5A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:51+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" .
}