@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP926494.RA75T6uNqV7xuMIXDJKuf5C0EjueoTgiwJYbulmGNqgKk
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP926494.RA75T6uNqV7xuMIXDJKuf5C0EjueoTgiwJYbulmGNqgKk130_head
{
this:
np:hasAssertion
dgn-np:NP926494.RA75T6uNqV7xuMIXDJKuf5C0EjueoTgiwJYbulmGNqgKk130_assertion
;
np:hasProvenance
dgn-np:NP926494.RA75T6uNqV7xuMIXDJKuf5C0EjueoTgiwJYbulmGNqgKk130_provenance
;
np:hasPublicationInfo
dgn-np:NP926494.RA75T6uNqV7xuMIXDJKuf5C0EjueoTgiwJYbulmGNqgKk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP926494.RA75T6uNqV7xuMIXDJKuf5C0EjueoTgiwJYbulmGNqgKk130_assertion
a
np:Assertion
.
dgn-np:NP926494.RA75T6uNqV7xuMIXDJKuf5C0EjueoTgiwJYbulmGNqgKk130_provenance
a
np:Provenance
.
dgn-np:NP926494.RA75T6uNqV7xuMIXDJKuf5C0EjueoTgiwJYbulmGNqgKk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP926494.RA75T6uNqV7xuMIXDJKuf5C0EjueoTgiwJYbulmGNqgKk130_assertion
{
miriam-gene:4928
a
ncit:C16612
.
lld:C0023467
a
ncit:C7057
.
dgn-gda:DGN853cb1dbf104a800c94085e4eef3fe3b
sio:SIO_000628
miriam-gene:4928
,
lld:C0023467
;
a
sio:SIO_001121
.
}
dgn-np:NP926494.RA75T6uNqV7xuMIXDJKuf5C0EjueoTgiwJYbulmGNqgKk130_provenance
{
dgn-np:NP926494.RA75T6uNqV7xuMIXDJKuf5C0EjueoTgiwJYbulmGNqgKk130_assertion
dcterms:description
"[NUP98 is known to be fused to at least 28 different partner genes in patients with hematopoietic malignancies, including acute myeloid leukemia, chronic myeloid leukemia in blast crisis, myelodysplastic syndrome, acute lymphoblastic leukemia, and bilineage/biphenotypic 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:21948299
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP926494.RA75T6uNqV7xuMIXDJKuf5C0EjueoTgiwJYbulmGNqgKk130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:45+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}