@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP540076.RAdWeywAsQCmASzvknWacgLO6aQV4Ji0VlD9EAX4GCJVc
> .
@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:NP540076.RAdWeywAsQCmASzvknWacgLO6aQV4Ji0VlD9EAX4GCJVc130_head
{
this:
np:hasAssertion
dgn-np:NP540076.RAdWeywAsQCmASzvknWacgLO6aQV4Ji0VlD9EAX4GCJVc130_assertion
;
np:hasProvenance
dgn-np:NP540076.RAdWeywAsQCmASzvknWacgLO6aQV4Ji0VlD9EAX4GCJVc130_provenance
;
np:hasPublicationInfo
dgn-np:NP540076.RAdWeywAsQCmASzvknWacgLO6aQV4Ji0VlD9EAX4GCJVc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP540076.RAdWeywAsQCmASzvknWacgLO6aQV4Ji0VlD9EAX4GCJVc130_assertion
a
np:Assertion
.
dgn-np:NP540076.RAdWeywAsQCmASzvknWacgLO6aQV4Ji0VlD9EAX4GCJVc130_provenance
a
np:Provenance
.
dgn-np:NP540076.RAdWeywAsQCmASzvknWacgLO6aQV4Ji0VlD9EAX4GCJVc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP540076.RAdWeywAsQCmASzvknWacgLO6aQV4Ji0VlD9EAX4GCJVc130_assertion
{
miriam-gene:4580
a
ncit:C16612
.
lld:C2697636
a
ncit:C7057
.
dgn-gda:DGN825a5fd6c8889e98182ee18517d6bde7
sio:SIO_000628
miriam-gene:4580
,
lld:C2697636
;
a
sio:SIO_001121
.
}
dgn-np:NP540076.RAdWeywAsQCmASzvknWacgLO6aQV4Ji0VlD9EAX4GCJVc130_provenance
{
dgn-np:NP540076.RAdWeywAsQCmASzvknWacgLO6aQV4Ji0VlD9EAX4GCJVc130_assertion
dcterms:description
"[Somatic mutations of the X-linked transcription factor gene, GATA1, have been detected uniformly and exclusively in DS AMkL cases, which may lead to altered expression of GATA1 target genes and alter the metabolism of drugs including ara-C. Hyperdiploid acute lymphoblastic leukemia (ALL) cells with extra copies of chromosome 21, generate higher levels of the active methotrexate (MTX) metabolite, MTX polyglutamates.]. 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:15390307
;
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:NP540076.RAdWeywAsQCmASzvknWacgLO6aQV4Ji0VlD9EAX4GCJVc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:25+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" .
}