@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP708104.RAqpSq50RyQOsrNnanIbbs_40V5z60od0BiPoAAy_8uaA
> .
@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/
> .
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{
this:
np:hasAssertion
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;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP708104.RAqpSq50RyQOsrNnanIbbs_40V5z60od0BiPoAAy_8uaA130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP708104.RAqpSq50RyQOsrNnanIbbs_40V5z60od0BiPoAAy_8uaA130_assertion
a
np:Assertion
.
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a
np:Provenance
.
dgn-np:NP708104.RAqpSq50RyQOsrNnanIbbs_40V5z60od0BiPoAAy_8uaA130_publicationInfo
a
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.
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{
miriam-gene:1636
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGN9c7961f3ebf99af89e28589efebafbf4
sio:SIO_000628
miriam-gene:1636
,
lld:C0020538
;
a
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.
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dgn-np:NP708104.RAqpSq50RyQOsrNnanIbbs_40V5z60od0BiPoAAy_8uaA130_provenance
{
dgn-np:NP708104.RAqpSq50RyQOsrNnanIbbs_40V5z60od0BiPoAAy_8uaA130_assertion
dcterms:description
"[Our study also showed that deletion in intron 16 of the ACE gene, which is associated with susceptibility to hypertension and variation of response to ACE inhibitors, can be found in all considered cells but Kyn2 cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
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sio:SIO_000772
miriam-pubmed:19067187
;
prov:wasDerivedFrom
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;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
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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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dgn-np:NP708104.RAqpSq50RyQOsrNnanIbbs_40V5z60od0BiPoAAy_8uaA130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:06+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
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pav:authoredBy
<
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> , <
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> , <
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> , <
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> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
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"v4.0.0" .
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