@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP436488.RA3wKo8c2UynxnExyDN9769P7j0nQptVS8nYrRbQyHJ2I
> .
@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:NP436488.RA3wKo8c2UynxnExyDN9769P7j0nQptVS8nYrRbQyHJ2I130_head
{
this:
np:hasAssertion
dgn-np:NP436488.RA3wKo8c2UynxnExyDN9769P7j0nQptVS8nYrRbQyHJ2I130_assertion
;
np:hasProvenance
dgn-np:NP436488.RA3wKo8c2UynxnExyDN9769P7j0nQptVS8nYrRbQyHJ2I130_provenance
;
np:hasPublicationInfo
dgn-np:NP436488.RA3wKo8c2UynxnExyDN9769P7j0nQptVS8nYrRbQyHJ2I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP436488.RA3wKo8c2UynxnExyDN9769P7j0nQptVS8nYrRbQyHJ2I130_assertion
a
np:Assertion
.
dgn-np:NP436488.RA3wKo8c2UynxnExyDN9769P7j0nQptVS8nYrRbQyHJ2I130_provenance
a
np:Provenance
.
dgn-np:NP436488.RA3wKo8c2UynxnExyDN9769P7j0nQptVS8nYrRbQyHJ2I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP436488.RA3wKo8c2UynxnExyDN9769P7j0nQptVS8nYrRbQyHJ2I130_assertion
{
miriam-gene:6929
a
ncit:C16612
.
lld:C0023418
a
ncit:C7057
.
dgn-gda:DGN571b5aa20aa9016e7ab9e7d0c641f3aa
sio:SIO_000628
miriam-gene:6929
,
lld:C0023418
;
a
sio:SIO_001121
.
}
dgn-np:NP436488.RA3wKo8c2UynxnExyDN9769P7j0nQptVS8nYrRbQyHJ2I130_provenance
{
dgn-np:NP436488.RA3wKo8c2UynxnExyDN9769P7j0nQptVS8nYrRbQyHJ2I130_assertion
dcterms:description
"[Since the E2A, PBX1 and HLF proteins all appear to function as transcription factors, it appears likely that the oncogenic fusion proteins contribute to leukemia development by causing abnormal transcriptional regulation of key target genes.]. 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:12700034
;
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:NP436488.RA3wKo8c2UynxnExyDN9769P7j0nQptVS8nYrRbQyHJ2I130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:18+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" .
}