@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP600937.RA69nZ1vjmvUWV9_60aggATgy0LxpE2DmuSScEx9phC4I
> .
@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/v3.0.0/void/
> .
dgn-np:NP600937.RA69nZ1vjmvUWV9_60aggATgy0LxpE2DmuSScEx9phC4I130_head
{
this:
np:hasAssertion
dgn-np:NP600937.RA69nZ1vjmvUWV9_60aggATgy0LxpE2DmuSScEx9phC4I130_assertion
;
np:hasProvenance
dgn-np:NP600937.RA69nZ1vjmvUWV9_60aggATgy0LxpE2DmuSScEx9phC4I130_provenance
;
np:hasPublicationInfo
dgn-np:NP600937.RA69nZ1vjmvUWV9_60aggATgy0LxpE2DmuSScEx9phC4I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP600937.RA69nZ1vjmvUWV9_60aggATgy0LxpE2DmuSScEx9phC4I130_assertion
a
np:Assertion
.
dgn-np:NP600937.RA69nZ1vjmvUWV9_60aggATgy0LxpE2DmuSScEx9phC4I130_provenance
a
np:Provenance
.
dgn-np:NP600937.RA69nZ1vjmvUWV9_60aggATgy0LxpE2DmuSScEx9phC4I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP600937.RA69nZ1vjmvUWV9_60aggATgy0LxpE2DmuSScEx9phC4I130_assertion
{
miriam-gene:4928
a
ncit:C16612
.
lld:C0005699
a
ncit:C7057
.
dgn-gda:DGNb6017cdf0f97dbe33fd760791a0b9f77
sio:SIO_000628
miriam-gene:4928
,
lld:C0005699
;
a
sio:SIO_001121
.
}
dgn-np:NP600937.RA69nZ1vjmvUWV9_60aggATgy0LxpE2DmuSScEx9phC4I130_provenance
{
dgn-np:NP600937.RA69nZ1vjmvUWV9_60aggATgy0LxpE2DmuSScEx9phC4I130_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-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP600937.RA69nZ1vjmvUWV9_60aggATgy0LxpE2DmuSScEx9phC4I130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:43:39+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}