@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP210920.RAn3WcKNE4Ezs-ho1OmhZMu-2VNst4C0kGxUKKmkL5I4w
> .
@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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{
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np:hasAssertion
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;
np:hasProvenance
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np:Nanopublication
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a
np:Assertion
.
dgn-np:NP210920.RAn3WcKNE4Ezs-ho1OmhZMu-2VNst4C0kGxUKKmkL5I4w130_provenance
a
np:Provenance
.
dgn-np:NP210920.RAn3WcKNE4Ezs-ho1OmhZMu-2VNst4C0kGxUKKmkL5I4w130_publicationInfo
a
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.
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{
miriam-gene:285335
a
ncit:C16612
.
lld:C0035078
a
ncit:C7057
.
dgn-gda:DGN7cc61eeab0d23ae2cd4bdd1ace1d3c6f
sio:SIO_000628
miriam-gene:285335
,
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.
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dgn-np:NP210920.RAn3WcKNE4Ezs-ho1OmhZMu-2VNst4C0kGxUKKmkL5I4w130_provenance
{
dgn-np:NP210920.RAn3WcKNE4Ezs-ho1OmhZMu-2VNst4C0kGxUKKmkL5I4w130_assertion
dcterms:description
"[The NHE primers and associated polymorphic loci identified in this study can be used in genomic, linkage, and association analysis of NHE genes in future genetic studies of hypertension and renal failure.]. 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:10642288
;
prov:wasDerivedFrom
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;
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 .
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{
this:
dcterms:created
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xsd:dateTime
;
dcterms:rights
<
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> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
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pav:authoredBy
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> , <
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