@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP631962.RAfjCrZP-_e80_B-qZuJxyBca_szIaDKgYjt-nYZR8cJs
> .
@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:NP631962.RAfjCrZP-_e80_B-qZuJxyBca_szIaDKgYjt-nYZR8cJs130_head
{
this:
np:hasAssertion
dgn-np:NP631962.RAfjCrZP-_e80_B-qZuJxyBca_szIaDKgYjt-nYZR8cJs130_assertion
;
np:hasProvenance
dgn-np:NP631962.RAfjCrZP-_e80_B-qZuJxyBca_szIaDKgYjt-nYZR8cJs130_provenance
;
np:hasPublicationInfo
dgn-np:NP631962.RAfjCrZP-_e80_B-qZuJxyBca_szIaDKgYjt-nYZR8cJs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP631962.RAfjCrZP-_e80_B-qZuJxyBca_szIaDKgYjt-nYZR8cJs130_assertion
a
np:Assertion
.
dgn-np:NP631962.RAfjCrZP-_e80_B-qZuJxyBca_szIaDKgYjt-nYZR8cJs130_provenance
a
np:Provenance
.
dgn-np:NP631962.RAfjCrZP-_e80_B-qZuJxyBca_szIaDKgYjt-nYZR8cJs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP631962.RAfjCrZP-_e80_B-qZuJxyBca_szIaDKgYjt-nYZR8cJs130_assertion
{
miriam-gene:1662
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN36a3508b3a3b448d9c5a328ef4e72e1f
sio:SIO_000628
miriam-gene:1662
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP631962.RAfjCrZP-_e80_B-qZuJxyBca_szIaDKgYjt-nYZR8cJs130_provenance
{
dgn-np:NP631962.RAfjCrZP-_e80_B-qZuJxyBca_szIaDKgYjt-nYZR8cJs130_assertion
dcterms:description
"[Genes of the HOXA cluster and the nuclear-receptor set domain (NSD) genes were frequently fused to NUP98, mainly in de novo myeloid malignancies whereas the DDX10 and TOP1 genes were equally rearranged in de novo and in therapy-related myeloid proliferations.]. 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:16467868
;
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:NP631962.RAfjCrZP-_e80_B-qZuJxyBca_szIaDKgYjt-nYZR8cJs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:21+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" .
}