@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP222683.RAWObUCpHrpSadCf5bIQGAe58f_Fa9_TCCh9qtw-mUCoQ
> .
@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:NP222683.RAWObUCpHrpSadCf5bIQGAe58f_Fa9_TCCh9qtw-mUCoQ130_head
{
this:
np:hasAssertion
dgn-np:NP222683.RAWObUCpHrpSadCf5bIQGAe58f_Fa9_TCCh9qtw-mUCoQ130_assertion
;
np:hasProvenance
dgn-np:NP222683.RAWObUCpHrpSadCf5bIQGAe58f_Fa9_TCCh9qtw-mUCoQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP222683.RAWObUCpHrpSadCf5bIQGAe58f_Fa9_TCCh9qtw-mUCoQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP222683.RAWObUCpHrpSadCf5bIQGAe58f_Fa9_TCCh9qtw-mUCoQ130_assertion
a
np:Assertion
.
dgn-np:NP222683.RAWObUCpHrpSadCf5bIQGAe58f_Fa9_TCCh9qtw-mUCoQ130_provenance
a
np:Provenance
.
dgn-np:NP222683.RAWObUCpHrpSadCf5bIQGAe58f_Fa9_TCCh9qtw-mUCoQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP222683.RAWObUCpHrpSadCf5bIQGAe58f_Fa9_TCCh9qtw-mUCoQ130_assertion
{
miriam-gene:2120
a
ncit:C16612
.
lld:C0023452
a
ncit:C7057
.
dgn-gda:DGN7809ab28ca55caa36c5eb55029155033
sio:SIO_000628
miriam-gene:2120
,
lld:C0023452
;
a
sio:SIO_001121
.
}
dgn-np:NP222683.RAWObUCpHrpSadCf5bIQGAe58f_Fa9_TCCh9qtw-mUCoQ130_provenance
{
dgn-np:NP222683.RAWObUCpHrpSadCf5bIQGAe58f_Fa9_TCCh9qtw-mUCoQ130_assertion
dcterms:description
"[Despite its rarity by routine karyotypic analysis, cryptic t(12;21)(p12-13;q22) translocation leading to TEL/AML1 fusion has been recognized as the most frequent genetic rearrangement in childhood acute lymphoblastic leukemia (ALL) in two recent studies, one from France and the other from the United States.]. 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:8667657
;
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:NP222683.RAWObUCpHrpSadCf5bIQGAe58f_Fa9_TCCh9qtw-mUCoQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:03+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" .
}