@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP185316.RAYMLhs6aWYFecUXxyn3nOKzgOcCtXK5m41fzVp3bntNI
> .
@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:NP185316.RAYMLhs6aWYFecUXxyn3nOKzgOcCtXK5m41fzVp3bntNI130_head
{
this:
np:hasAssertion
dgn-np:NP185316.RAYMLhs6aWYFecUXxyn3nOKzgOcCtXK5m41fzVp3bntNI130_assertion
;
np:hasProvenance
dgn-np:NP185316.RAYMLhs6aWYFecUXxyn3nOKzgOcCtXK5m41fzVp3bntNI130_provenance
;
np:hasPublicationInfo
dgn-np:NP185316.RAYMLhs6aWYFecUXxyn3nOKzgOcCtXK5m41fzVp3bntNI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP185316.RAYMLhs6aWYFecUXxyn3nOKzgOcCtXK5m41fzVp3bntNI130_assertion
a
np:Assertion
.
dgn-np:NP185316.RAYMLhs6aWYFecUXxyn3nOKzgOcCtXK5m41fzVp3bntNI130_provenance
a
np:Provenance
.
dgn-np:NP185316.RAYMLhs6aWYFecUXxyn3nOKzgOcCtXK5m41fzVp3bntNI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP185316.RAYMLhs6aWYFecUXxyn3nOKzgOcCtXK5m41fzVp3bntNI130_assertion
{
miriam-gene:4211
a
ncit:C16612
.
lld:C0023418
a
ncit:C7057
.
dgn-gda:DGN79a3708bbb9d83ecf708f5e6f5c10be1
sio:SIO_000628
miriam-gene:4211
,
lld:C0023418
;
a
sio:SIO_001121
.
}
dgn-np:NP185316.RAYMLhs6aWYFecUXxyn3nOKzgOcCtXK5m41fzVp3bntNI130_provenance
{
dgn-np:NP185316.RAYMLhs6aWYFecUXxyn3nOKzgOcCtXK5m41fzVp3bntNI130_assertion
dcterms:description
"[Phylogenetic sequence analysis and reporter assays in MEIS1-expressing (K562) and nonexpressing (HL60) leukemic cell line models were used to identify key regulatory regions and potential transcription factor binding sites within the candidate promoter region followed by functional and expression studies of one identified regulator in both cell lines and primary human cord blood and leukemia samples.]. 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:20600580
;
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:NP185316.RAYMLhs6aWYFecUXxyn3nOKzgOcCtXK5m41fzVp3bntNI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:41+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" .
}