@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP220290.RAiDV8r8r9i12tQVI9tDcRP0oY7oMKKSiW5vCccrUspDI
> .
@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:NP220290.RAiDV8r8r9i12tQVI9tDcRP0oY7oMKKSiW5vCccrUspDI130_head
{
this:
np:hasAssertion
dgn-np:NP220290.RAiDV8r8r9i12tQVI9tDcRP0oY7oMKKSiW5vCccrUspDI130_assertion
;
np:hasProvenance
dgn-np:NP220290.RAiDV8r8r9i12tQVI9tDcRP0oY7oMKKSiW5vCccrUspDI130_provenance
;
np:hasPublicationInfo
dgn-np:NP220290.RAiDV8r8r9i12tQVI9tDcRP0oY7oMKKSiW5vCccrUspDI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP220290.RAiDV8r8r9i12tQVI9tDcRP0oY7oMKKSiW5vCccrUspDI130_assertion
a
np:Assertion
.
dgn-np:NP220290.RAiDV8r8r9i12tQVI9tDcRP0oY7oMKKSiW5vCccrUspDI130_provenance
a
np:Provenance
.
dgn-np:NP220290.RAiDV8r8r9i12tQVI9tDcRP0oY7oMKKSiW5vCccrUspDI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP220290.RAiDV8r8r9i12tQVI9tDcRP0oY7oMKKSiW5vCccrUspDI130_assertion
{
miriam-gene:1029
a
ncit:C16612
.
lld:C0023452
a
ncit:C7057
.
dgn-gda:DGNe0cf0bfd21a776ed49112f1eb7a96200
sio:SIO_000628
miriam-gene:1029
,
lld:C0023452
;
a
sio:SIO_001121
.
}
dgn-np:NP220290.RAiDV8r8r9i12tQVI9tDcRP0oY7oMKKSiW5vCccrUspDI130_provenance
{
dgn-np:NP220290.RAiDV8r8r9i12tQVI9tDcRP0oY7oMKKSiW5vCccrUspDI130_assertion
dcterms:description
"[To determine the frequency and prognostic significance of recently described genetic lesions in pediatric acute lymphoblastic leukemia (ALL), all cases with available leukemic cell samples treated on St Jude Study XII were analyzed by molecular techniques for alterations of the p16, MLL and ETV6 genes.]. 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:9264370
;
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:NP220290.RAiDV8r8r9i12tQVI9tDcRP0oY7oMKKSiW5vCccrUspDI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:02+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" .
}