@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP831100.RAotqSSJxtqAsPTeZUBbwrmyJXuW-rvQGXzLD4ItEXwnI
> .
@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:NP831100.RAotqSSJxtqAsPTeZUBbwrmyJXuW-rvQGXzLD4ItEXwnI130_head
{
this:
np:hasAssertion
dgn-np:NP831100.RAotqSSJxtqAsPTeZUBbwrmyJXuW-rvQGXzLD4ItEXwnI130_assertion
;
np:hasProvenance
dgn-np:NP831100.RAotqSSJxtqAsPTeZUBbwrmyJXuW-rvQGXzLD4ItEXwnI130_provenance
;
np:hasPublicationInfo
dgn-np:NP831100.RAotqSSJxtqAsPTeZUBbwrmyJXuW-rvQGXzLD4ItEXwnI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP831100.RAotqSSJxtqAsPTeZUBbwrmyJXuW-rvQGXzLD4ItEXwnI130_assertion
a
np:Assertion
.
dgn-np:NP831100.RAotqSSJxtqAsPTeZUBbwrmyJXuW-rvQGXzLD4ItEXwnI130_provenance
a
np:Provenance
.
dgn-np:NP831100.RAotqSSJxtqAsPTeZUBbwrmyJXuW-rvQGXzLD4ItEXwnI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP831100.RAotqSSJxtqAsPTeZUBbwrmyJXuW-rvQGXzLD4ItEXwnI130_assertion
{
miriam-gene:2057
a
ncit:C16612
.
lld:C0741916
a
ncit:C7057
.
dgn-gda:DGNf8b29c24923aedf9ab136b5583013a6f
sio:SIO_000628
miriam-gene:2057
,
lld:C0741916
;
a
sio:SIO_001121
.
}
dgn-np:NP831100.RAotqSSJxtqAsPTeZUBbwrmyJXuW-rvQGXzLD4ItEXwnI130_provenance
{
dgn-np:NP831100.RAotqSSJxtqAsPTeZUBbwrmyJXuW-rvQGXzLD4ItEXwnI130_assertion
dcterms:description
"[In addition to restoration of erythropoiesis during development, the cardiac defect associated with embryos lacking the erythropoietin receptor was corrected and the increased apoptosis in fetal liver, heart, and brain in the erythropoietin receptor null phenotype was markedly reduced.]. 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:11435319
;
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:NP831100.RAotqSSJxtqAsPTeZUBbwrmyJXuW-rvQGXzLD4ItEXwnI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:28+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" .
}