@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP289942.RAx1ZvbsEsLx2o8lHvX7nn2F83PL1ZuzTZcVpWkshVmM0
> .
@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:NP289942.RAx1ZvbsEsLx2o8lHvX7nn2F83PL1ZuzTZcVpWkshVmM0130_head
{
this:
np:hasAssertion
dgn-np:NP289942.RAx1ZvbsEsLx2o8lHvX7nn2F83PL1ZuzTZcVpWkshVmM0130_assertion
;
np:hasProvenance
dgn-np:NP289942.RAx1ZvbsEsLx2o8lHvX7nn2F83PL1ZuzTZcVpWkshVmM0130_provenance
;
np:hasPublicationInfo
dgn-np:NP289942.RAx1ZvbsEsLx2o8lHvX7nn2F83PL1ZuzTZcVpWkshVmM0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP289942.RAx1ZvbsEsLx2o8lHvX7nn2F83PL1ZuzTZcVpWkshVmM0130_assertion
a
np:Assertion
.
dgn-np:NP289942.RAx1ZvbsEsLx2o8lHvX7nn2F83PL1ZuzTZcVpWkshVmM0130_provenance
a
np:Provenance
.
dgn-np:NP289942.RAx1ZvbsEsLx2o8lHvX7nn2F83PL1ZuzTZcVpWkshVmM0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP289942.RAx1ZvbsEsLx2o8lHvX7nn2F83PL1ZuzTZcVpWkshVmM0130_assertion
{
miriam-gene:116085
a
ncit:C16612
.
lld:C0392525
a
ncit:C7057
.
dgn-gda:DGN316247403309eaaef0e420d2df7687dd
sio:SIO_000628
miriam-gene:116085
,
lld:C0392525
;
a
sio:SIO_001121
.
}
dgn-np:NP289942.RAx1ZvbsEsLx2o8lHvX7nn2F83PL1ZuzTZcVpWkshVmM0130_provenance
{
dgn-np:NP289942.RAx1ZvbsEsLx2o8lHvX7nn2F83PL1ZuzTZcVpWkshVmM0130_assertion
dcterms:description
"[This data highlights the importance of the URAT1 renal urate transporter in determining serum urate concentrations and the clinical phenotypes, including nephrolithiasis, that should prompt the clinician to suspect an inherited form of renal hypouricaemia.]. 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:22194875
;
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:NP289942.RAx1ZvbsEsLx2o8lHvX7nn2F83PL1ZuzTZcVpWkshVmM0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:45+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" .
}