@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP378320.RAwRBURNA9wBFE35ZVc-We0ptIG7OKCSRNHlkHbGRDjeA
> .
@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/v3.0.0/void/
> .
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{
this:
np:hasAssertion
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;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP378320.RAwRBURNA9wBFE35ZVc-We0ptIG7OKCSRNHlkHbGRDjeA130_publicationInfo
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a
np:Nanopublication
.
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a
np:Assertion
.
dgn-np:NP378320.RAwRBURNA9wBFE35ZVc-We0ptIG7OKCSRNHlkHbGRDjeA130_provenance
a
np:Provenance
.
dgn-np:NP378320.RAwRBURNA9wBFE35ZVc-We0ptIG7OKCSRNHlkHbGRDjeA130_publicationInfo
a
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{
miriam-gene:2056
a
ncit:C16612
.
lld:C1527405
a
ncit:C7057
.
dgn-gda:DGN54d7b624b23482e92b1256db60073845
sio:SIO_000628
miriam-gene:2056
,
lld:C1527405
;
a
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.
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dgn-np:NP378320.RAwRBURNA9wBFE35ZVc-We0ptIG7OKCSRNHlkHbGRDjeA130_provenance
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dgn-np:NP378320.RAwRBURNA9wBFE35ZVc-We0ptIG7OKCSRNHlkHbGRDjeA130_assertion
dcterms:description
"[Here, we describe a novel mouse line with conditional PHD2 inactivation (cKO P2) in renal EPO producing cells, neurons, and astrocytes that displayed excessive erythrocytosis because of severe overproduction of EPO, exclusively driven by HIF-2α.]. 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:23264599
;
prov:wasDerivedFrom
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;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP378320.RAwRBURNA9wBFE35ZVc-We0ptIG7OKCSRNHlkHbGRDjeA130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:41:18+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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<
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> , <
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> , <
http://orcid.org/0000-0003-0169-8159
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> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
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pav:version
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"v3.0.0" .
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