@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP883240.RAwyrTVaQUdkAAqufd0XujgHBLEISwhM-j_H7kVQI_ANI
> .
@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:NP883240.RAwyrTVaQUdkAAqufd0XujgHBLEISwhM-j_H7kVQI_ANI130_head
{
this:
np:hasAssertion
dgn-np:NP883240.RAwyrTVaQUdkAAqufd0XujgHBLEISwhM-j_H7kVQI_ANI130_assertion
;
np:hasProvenance
dgn-np:NP883240.RAwyrTVaQUdkAAqufd0XujgHBLEISwhM-j_H7kVQI_ANI130_provenance
;
np:hasPublicationInfo
dgn-np:NP883240.RAwyrTVaQUdkAAqufd0XujgHBLEISwhM-j_H7kVQI_ANI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP883240.RAwyrTVaQUdkAAqufd0XujgHBLEISwhM-j_H7kVQI_ANI130_assertion
a
np:Assertion
.
dgn-np:NP883240.RAwyrTVaQUdkAAqufd0XujgHBLEISwhM-j_H7kVQI_ANI130_provenance
a
np:Provenance
.
dgn-np:NP883240.RAwyrTVaQUdkAAqufd0XujgHBLEISwhM-j_H7kVQI_ANI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP883240.RAwyrTVaQUdkAAqufd0XujgHBLEISwhM-j_H7kVQI_ANI130_assertion
{
miriam-gene:199699
a
ncit:C16612
.
lld:C0003873
a
ncit:C7057
.
dgn-gda:DGN99aef857c63d2a9c1ecb4832f482820d
sio:SIO_000628
miriam-gene:199699
,
lld:C0003873
;
a
sio:SIO_001121
.
}
dgn-np:NP883240.RAwyrTVaQUdkAAqufd0XujgHBLEISwhM-j_H7kVQI_ANI130_provenance
{
dgn-np:NP883240.RAwyrTVaQUdkAAqufd0XujgHBLEISwhM-j_H7kVQI_ANI130_assertion
dcterms:description
"[A luciferase-reporter gene assay and gel shift assay demonstrated that RUNX1, which is an essential hematopoietic transcription factor associated with acute myeloid leukemia and is related to RA and Sp1, is involved in the regulation of OCTN1 promoter activity.]. 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:17142562
;
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:NP883240.RAwyrTVaQUdkAAqufd0XujgHBLEISwhM-j_H7kVQI_ANI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:59+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" .
}