@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP498186.RA6x7-Q_VwUr-8lwKTK57Qom0089ZL8zv1Dkw2kMzs4zk
> .
@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:NP498186.RA6x7-Q_VwUr-8lwKTK57Qom0089ZL8zv1Dkw2kMzs4zk130_head
{
this:
np:hasAssertion
dgn-np:NP498186.RA6x7-Q_VwUr-8lwKTK57Qom0089ZL8zv1Dkw2kMzs4zk130_assertion
;
np:hasProvenance
dgn-np:NP498186.RA6x7-Q_VwUr-8lwKTK57Qom0089ZL8zv1Dkw2kMzs4zk130_provenance
;
np:hasPublicationInfo
dgn-np:NP498186.RA6x7-Q_VwUr-8lwKTK57Qom0089ZL8zv1Dkw2kMzs4zk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP498186.RA6x7-Q_VwUr-8lwKTK57Qom0089ZL8zv1Dkw2kMzs4zk130_assertion
a
np:Assertion
.
dgn-np:NP498186.RA6x7-Q_VwUr-8lwKTK57Qom0089ZL8zv1Dkw2kMzs4zk130_provenance
a
np:Provenance
.
dgn-np:NP498186.RA6x7-Q_VwUr-8lwKTK57Qom0089ZL8zv1Dkw2kMzs4zk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP498186.RA6x7-Q_VwUr-8lwKTK57Qom0089ZL8zv1Dkw2kMzs4zk130_assertion
{
miriam-gene:2624
a
ncit:C16612
.
lld:C0598766
a
ncit:C7057
.
dgn-gda:DGN9b15d5ce916c34db43f19a066bb7378f
sio:SIO_000628
miriam-gene:2624
,
lld:C0598766
;
a
sio:SIO_001121
.
}
dgn-np:NP498186.RA6x7-Q_VwUr-8lwKTK57Qom0089ZL8zv1Dkw2kMzs4zk130_provenance
{
dgn-np:NP498186.RA6x7-Q_VwUr-8lwKTK57Qom0089ZL8zv1Dkw2kMzs4zk130_assertion
dcterms:description
"[Results of GATA-2 expression analyses in leukemic cell lines as well as primary patient samples are compatible with the hypothesis that 3q21 aberrations contribute to leukemogenesis through deregulation of the hematopoietic transcription factor GATA-2.]. 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:10873593
;
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:NP498186.RA6x7-Q_VwUr-8lwKTK57Qom0089ZL8zv1Dkw2kMzs4zk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:57+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" .
}