@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP400657.RAL7nNr5RFwUfG4EwPLRAzRpOzFSDoDVaJAc4QNkIkHRk
> .
@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:NP400657.RAL7nNr5RFwUfG4EwPLRAzRpOzFSDoDVaJAc4QNkIkHRk130_head
{
this:
np:hasAssertion
dgn-np:NP400657.RAL7nNr5RFwUfG4EwPLRAzRpOzFSDoDVaJAc4QNkIkHRk130_assertion
;
np:hasProvenance
dgn-np:NP400657.RAL7nNr5RFwUfG4EwPLRAzRpOzFSDoDVaJAc4QNkIkHRk130_provenance
;
np:hasPublicationInfo
dgn-np:NP400657.RAL7nNr5RFwUfG4EwPLRAzRpOzFSDoDVaJAc4QNkIkHRk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP400657.RAL7nNr5RFwUfG4EwPLRAzRpOzFSDoDVaJAc4QNkIkHRk130_assertion
a
np:Assertion
.
dgn-np:NP400657.RAL7nNr5RFwUfG4EwPLRAzRpOzFSDoDVaJAc4QNkIkHRk130_provenance
a
np:Provenance
.
dgn-np:NP400657.RAL7nNr5RFwUfG4EwPLRAzRpOzFSDoDVaJAc4QNkIkHRk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP400657.RAL7nNr5RFwUfG4EwPLRAzRpOzFSDoDVaJAc4QNkIkHRk130_assertion
{
miriam-gene:10726
a
ncit:C16612
.
lld:C1961102
a
ncit:C7057
.
dgn-gda:DGN1c917ad9c108a9253c69ef516231620e
sio:SIO_000628
miriam-gene:10726
,
lld:C1961102
;
a
sio:SIO_001121
.
}
dgn-np:NP400657.RAL7nNr5RFwUfG4EwPLRAzRpOzFSDoDVaJAc4QNkIkHRk130_provenance
{
dgn-np:NP400657.RAL7nNr5RFwUfG4EwPLRAzRpOzFSDoDVaJAc4QNkIkHRk130_assertion
dcterms:description
"[A significant increase in HNUDC is present in bone marrow aspirates from patients with acute lymphoblastic leukemia (ALL) and acute myelogenous leukemia (AML) compared to the level in normal cellular counterparts, demonstrating dysregulated expression in leukemia.]. 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:11342328
;
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:NP400657.RAL7nNr5RFwUfG4EwPLRAzRpOzFSDoDVaJAc4QNkIkHRk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:58+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" .
}