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http://rdf.disgenet.org/nanopublications.trig#NP755927.RATtBuPt1FTNGMc7_darh7CSLLNVQpCxi-u3Kh504r0YA
> .
@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:NP755927.RATtBuPt1FTNGMc7_darh7CSLLNVQpCxi-u3Kh504r0YA130_head
{
this:
np:hasAssertion
dgn-np:NP755927.RATtBuPt1FTNGMc7_darh7CSLLNVQpCxi-u3Kh504r0YA130_assertion
;
np:hasProvenance
dgn-np:NP755927.RATtBuPt1FTNGMc7_darh7CSLLNVQpCxi-u3Kh504r0YA130_provenance
;
np:hasPublicationInfo
dgn-np:NP755927.RATtBuPt1FTNGMc7_darh7CSLLNVQpCxi-u3Kh504r0YA130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP755927.RATtBuPt1FTNGMc7_darh7CSLLNVQpCxi-u3Kh504r0YA130_assertion
a
np:Assertion
.
dgn-np:NP755927.RATtBuPt1FTNGMc7_darh7CSLLNVQpCxi-u3Kh504r0YA130_provenance
a
np:Provenance
.
dgn-np:NP755927.RATtBuPt1FTNGMc7_darh7CSLLNVQpCxi-u3Kh504r0YA130_publicationInfo
a
np:PublicationInfo
.
}
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{
miriam-gene:10320
a
ncit:C16612
.
lld:C0023452
a
ncit:C7057
.
dgn-gda:DGN6019e09b0182b382f69d8bfffab256f3
sio:SIO_000628
miriam-gene:10320
,
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;
a
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.
}
dgn-np:NP755927.RATtBuPt1FTNGMc7_darh7CSLLNVQpCxi-u3Kh504r0YA130_provenance
{
dgn-np:NP755927.RATtBuPt1FTNGMc7_darh7CSLLNVQpCxi-u3Kh504r0YA130_assertion
dcterms:description
"[Recent genome-wide association studies (GWAS) that focus on childhood acute lymphoblastic leukemia (ALL), the most common malignancy in children younger than 15 years old, have found evidence that single nucleotide polymorphisms (SNPs) in IKZF1 (7p12.2), ARID5B (10q21.2) and CEBPE (14q11.2) are strongly related to the risk of childhood ALL.]. 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:23608171
;
prov:wasDerivedFrom
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;
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:NP755927.RATtBuPt1FTNGMc7_darh7CSLLNVQpCxi-u3Kh504r0YA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:38+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
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<
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> , <
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> , <
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> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
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