@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP120581.RANQjAvmWAuy34tYJeatM7bPRkH0RT0vcSlbF6frv2UDc
> .
@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:NP120581.RANQjAvmWAuy34tYJeatM7bPRkH0RT0vcSlbF6frv2UDc130_head
{
this:
np:hasAssertion
dgn-np:NP120581.RANQjAvmWAuy34tYJeatM7bPRkH0RT0vcSlbF6frv2UDc130_assertion
;
np:hasProvenance
dgn-np:NP120581.RANQjAvmWAuy34tYJeatM7bPRkH0RT0vcSlbF6frv2UDc130_provenance
;
np:hasPublicationInfo
dgn-np:NP120581.RANQjAvmWAuy34tYJeatM7bPRkH0RT0vcSlbF6frv2UDc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP120581.RANQjAvmWAuy34tYJeatM7bPRkH0RT0vcSlbF6frv2UDc130_assertion
a
np:Assertion
.
dgn-np:NP120581.RANQjAvmWAuy34tYJeatM7bPRkH0RT0vcSlbF6frv2UDc130_provenance
a
np:Provenance
.
dgn-np:NP120581.RANQjAvmWAuy34tYJeatM7bPRkH0RT0vcSlbF6frv2UDc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP120581.RANQjAvmWAuy34tYJeatM7bPRkH0RT0vcSlbF6frv2UDc130_assertion
{
miriam-gene:7351
a
ncit:C16612
.
lld:C0003130
a
ncit:C7057
.
dgn-gda:DGN7d383af2793033d5498ca38a283e6ac2
sio:SIO_000628
miriam-gene:7351
,
lld:C0003130
;
a
sio:SIO_001123
.
}
dgn-np:NP120581.RANQjAvmWAuy34tYJeatM7bPRkH0RT0vcSlbF6frv2UDc130_provenance
{
dgn-np:NP120581.RANQjAvmWAuy34tYJeatM7bPRkH0RT0vcSlbF6frv2UDc130_assertion
dcterms:description
"[High UCP2 transcript levels were detected in reticulocytes and other maturating erythroid cells in mice exposed to hypoxia, and in umbilical cord blood of human neonates and peripheral blood of adults, suggesting involvement of UCP2 in erythropoiesis ]. 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:17316620
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP120581.RANQjAvmWAuy34tYJeatM7bPRkH0RT0vcSlbF6frv2UDc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:02+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" .
}