@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP559410.RAVY9BBXtNcZ_4C2kSCpdZMZXS0HJ7AB77myh9brgM7Ao
> .
@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:NP559410.RAVY9BBXtNcZ_4C2kSCpdZMZXS0HJ7AB77myh9brgM7Ao130_head
{
this:
np:hasAssertion
dgn-np:NP559410.RAVY9BBXtNcZ_4C2kSCpdZMZXS0HJ7AB77myh9brgM7Ao130_assertion
;
np:hasProvenance
dgn-np:NP559410.RAVY9BBXtNcZ_4C2kSCpdZMZXS0HJ7AB77myh9brgM7Ao130_provenance
;
np:hasPublicationInfo
dgn-np:NP559410.RAVY9BBXtNcZ_4C2kSCpdZMZXS0HJ7AB77myh9brgM7Ao130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP559410.RAVY9BBXtNcZ_4C2kSCpdZMZXS0HJ7AB77myh9brgM7Ao130_assertion
a
np:Assertion
.
dgn-np:NP559410.RAVY9BBXtNcZ_4C2kSCpdZMZXS0HJ7AB77myh9brgM7Ao130_provenance
a
np:Provenance
.
dgn-np:NP559410.RAVY9BBXtNcZ_4C2kSCpdZMZXS0HJ7AB77myh9brgM7Ao130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP559410.RAVY9BBXtNcZ_4C2kSCpdZMZXS0HJ7AB77myh9brgM7Ao130_assertion
{
miriam-gene:4297
a
ncit:C16612
.
lld:C2825306
a
ncit:C7057
.
dgn-gda:DGN1d5737671aa72b24ebb818f8745a0ef9
sio:SIO_000628
miriam-gene:4297
,
lld:C2825306
;
a
sio:SIO_001122
.
}
dgn-np:NP559410.RAVY9BBXtNcZ_4C2kSCpdZMZXS0HJ7AB77myh9brgM7Ao130_provenance
{
dgn-np:NP559410.RAVY9BBXtNcZ_4C2kSCpdZMZXS0HJ7AB77myh9brgM7Ao130_assertion
dcterms:description
"[The translocation t(9;11)(p22;q23), which results in the fusion of MLL to AF9, is the most common of the 11q23 chromosomal abnormalities observed in de novo acute myeloid leukemia (AML), in therapy related leukemia (t-AML), and rarely in acute lymphoblastic leukemia (ALL).]. 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:9331569
;
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:NP559410.RAVY9BBXtNcZ_4C2kSCpdZMZXS0HJ7AB77myh9brgM7Ao130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:43:12+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" .
}