@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP560231.RAB6wGiVH06EjvAGwMZMf8khUKPASd_imY4mrU-oxSRfI
> .
@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:NP560231.RAB6wGiVH06EjvAGwMZMf8khUKPASd_imY4mrU-oxSRfI130_head
{
this:
np:hasAssertion
dgn-np:NP560231.RAB6wGiVH06EjvAGwMZMf8khUKPASd_imY4mrU-oxSRfI130_assertion
;
np:hasProvenance
dgn-np:NP560231.RAB6wGiVH06EjvAGwMZMf8khUKPASd_imY4mrU-oxSRfI130_provenance
;
np:hasPublicationInfo
dgn-np:NP560231.RAB6wGiVH06EjvAGwMZMf8khUKPASd_imY4mrU-oxSRfI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP560231.RAB6wGiVH06EjvAGwMZMf8khUKPASd_imY4mrU-oxSRfI130_assertion
a
np:Assertion
.
dgn-np:NP560231.RAB6wGiVH06EjvAGwMZMf8khUKPASd_imY4mrU-oxSRfI130_provenance
a
np:Provenance
.
dgn-np:NP560231.RAB6wGiVH06EjvAGwMZMf8khUKPASd_imY4mrU-oxSRfI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP560231.RAB6wGiVH06EjvAGwMZMf8khUKPASd_imY4mrU-oxSRfI130_assertion
{
miriam-gene:617
a
ncit:C16612
.
lld:C0023418
a
ncit:C7057
.
dgn-gda:DGNd662c3364326d6a6dfea4a2661f3f36b
sio:SIO_000628
miriam-gene:617
,
lld:C0023418
;
a
sio:SIO_001121
.
}
dgn-np:NP560231.RAB6wGiVH06EjvAGwMZMf8khUKPASd_imY4mrU-oxSRfI130_provenance
{
dgn-np:NP560231.RAB6wGiVH06EjvAGwMZMf8khUKPASd_imY4mrU-oxSRfI130_assertion
dcterms:description
"[Among them, re-arrangements of the mixed lineage leukemia gene (MLL), including chimeric fusion, partial tandem duplication (PTD), amplification and internal exonic deletion, represent one of the most common recurring oncogenic events and associate with very poor prognosis in human leukemias.]. 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:23598978
;
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:NP560231.RAB6wGiVH06EjvAGwMZMf8khUKPASd_imY4mrU-oxSRfI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:38+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" .
}