@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP852124.RACte4TON5lOU4aFXrZizrKWmTU80fHw_VUGNdFIoHNCk
> .
@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:NP852124.RACte4TON5lOU4aFXrZizrKWmTU80fHw_VUGNdFIoHNCk130_head
{
this:
np:hasAssertion
dgn-np:NP852124.RACte4TON5lOU4aFXrZizrKWmTU80fHw_VUGNdFIoHNCk130_assertion
;
np:hasProvenance
dgn-np:NP852124.RACte4TON5lOU4aFXrZizrKWmTU80fHw_VUGNdFIoHNCk130_provenance
;
np:hasPublicationInfo
dgn-np:NP852124.RACte4TON5lOU4aFXrZizrKWmTU80fHw_VUGNdFIoHNCk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP852124.RACte4TON5lOU4aFXrZizrKWmTU80fHw_VUGNdFIoHNCk130_assertion
a
np:Assertion
.
dgn-np:NP852124.RACte4TON5lOU4aFXrZizrKWmTU80fHw_VUGNdFIoHNCk130_provenance
a
np:Provenance
.
dgn-np:NP852124.RACte4TON5lOU4aFXrZizrKWmTU80fHw_VUGNdFIoHNCk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP852124.RACte4TON5lOU4aFXrZizrKWmTU80fHw_VUGNdFIoHNCk130_assertion
{
miriam-gene:865
a
ncit:C16612
.
lld:C1961102
a
ncit:C7057
.
dgn-gda:DGN9874f765ae72e1f8d6634321e96a7ce3
sio:SIO_000628
miriam-gene:865
,
lld:C1961102
;
a
sio:SIO_001121
.
}
dgn-np:NP852124.RACte4TON5lOU4aFXrZizrKWmTU80fHw_VUGNdFIoHNCk130_provenance
{
dgn-np:NP852124.RACte4TON5lOU4aFXrZizrKWmTU80fHw_VUGNdFIoHNCk130_assertion
dcterms:description
"[This hypothesis was confirmed by the detection of deletions of the 3' regions of the CBFB and the MLL genes in AML M4 patients with inv(16) and in patients with ALL and AML associated with MLL gene translocations, respectively.]. 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:11369654
;
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:NP852124.RACte4TON5lOU4aFXrZizrKWmTU80fHw_VUGNdFIoHNCk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:40+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" .
}