@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP485495.RAqrnT2ADu3vd_xRKVDKjWPmZ4rHkkPVVsUG6A5D0DQhc
> .
@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:NP485495.RAqrnT2ADu3vd_xRKVDKjWPmZ4rHkkPVVsUG6A5D0DQhc130_head
{
this:
np:hasAssertion
dgn-np:NP485495.RAqrnT2ADu3vd_xRKVDKjWPmZ4rHkkPVVsUG6A5D0DQhc130_assertion
;
np:hasProvenance
dgn-np:NP485495.RAqrnT2ADu3vd_xRKVDKjWPmZ4rHkkPVVsUG6A5D0DQhc130_provenance
;
np:hasPublicationInfo
dgn-np:NP485495.RAqrnT2ADu3vd_xRKVDKjWPmZ4rHkkPVVsUG6A5D0DQhc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP485495.RAqrnT2ADu3vd_xRKVDKjWPmZ4rHkkPVVsUG6A5D0DQhc130_assertion
a
np:Assertion
.
dgn-np:NP485495.RAqrnT2ADu3vd_xRKVDKjWPmZ4rHkkPVVsUG6A5D0DQhc130_provenance
a
np:Provenance
.
dgn-np:NP485495.RAqrnT2ADu3vd_xRKVDKjWPmZ4rHkkPVVsUG6A5D0DQhc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP485495.RAqrnT2ADu3vd_xRKVDKjWPmZ4rHkkPVVsUG6A5D0DQhc130_assertion
{
miriam-gene:55120
a
ncit:C16612
.
lld:C0023449
a
ncit:C7057
.
dgn-gda:DGN58ca56f971391f752af27a03a5756fb5
sio:SIO_000628
miriam-gene:55120
,
lld:C0023449
;
a
sio:SIO_001121
.
}
dgn-np:NP485495.RAqrnT2ADu3vd_xRKVDKjWPmZ4rHkkPVVsUG6A5D0DQhc130_provenance
{
dgn-np:NP485495.RAqrnT2ADu3vd_xRKVDKjWPmZ4rHkkPVVsUG6A5D0DQhc130_assertion
dcterms:description
"[Presenting features and leukemic cell characteristics were compared for 76 patients with Down syndrome and 4,733 other patients with newly diagnosed ALL treated on protocols of the Pediatric Oncology Group (POG) and St Jude Children's Research Hospital (SJCRH).]. 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:8315434
;
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:NP485495.RAqrnT2ADu3vd_xRKVDKjWPmZ4rHkkPVVsUG6A5D0DQhc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:50+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" .
}