@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP834131.RAsIHc_smyfilspGNc1HOQ-m9sE8L_oNWM05FGMgxs9Bo
> .
@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:NP834131.RAsIHc_smyfilspGNc1HOQ-m9sE8L_oNWM05FGMgxs9Bo130_head
{
this:
np:hasAssertion
dgn-np:NP834131.RAsIHc_smyfilspGNc1HOQ-m9sE8L_oNWM05FGMgxs9Bo130_assertion
;
np:hasProvenance
dgn-np:NP834131.RAsIHc_smyfilspGNc1HOQ-m9sE8L_oNWM05FGMgxs9Bo130_provenance
;
np:hasPublicationInfo
dgn-np:NP834131.RAsIHc_smyfilspGNc1HOQ-m9sE8L_oNWM05FGMgxs9Bo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP834131.RAsIHc_smyfilspGNc1HOQ-m9sE8L_oNWM05FGMgxs9Bo130_assertion
a
np:Assertion
.
dgn-np:NP834131.RAsIHc_smyfilspGNc1HOQ-m9sE8L_oNWM05FGMgxs9Bo130_provenance
a
np:Provenance
.
dgn-np:NP834131.RAsIHc_smyfilspGNc1HOQ-m9sE8L_oNWM05FGMgxs9Bo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP834131.RAsIHc_smyfilspGNc1HOQ-m9sE8L_oNWM05FGMgxs9Bo130_assertion
{
miriam-gene:2623
a
ncit:C16612
.
lld:C0033027
a
ncit:C7057
.
dgn-gda:DGN61a70b81f2efcf9018b58e5e7e315533
sio:SIO_000628
miriam-gene:2623
,
lld:C0033027
;
a
sio:SIO_001121
.
}
dgn-np:NP834131.RAsIHc_smyfilspGNc1HOQ-m9sE8L_oNWM05FGMgxs9Bo130_provenance
{
dgn-np:NP834131.RAsIHc_smyfilspGNc1HOQ-m9sE8L_oNWM05FGMgxs9Bo130_assertion
dcterms:description
"[We earlier reported on a mouse model that constitutive expression of EVI1 in the BM led to fatal anemia and myeloid dysplasia, as observed in MDS patients, and we subsequently showed that EVI1 interaction with GATA1 blocks proper 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:19208846
;
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:NP834131.RAsIHc_smyfilspGNc1HOQ-m9sE8L_oNWM05FGMgxs9Bo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:30+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" .
}