@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP364499.RAophFrLr0dJIusd_riUHm5OQj-yq3Ha89UXn7DjQWsvI
> .
@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:NP364499.RAophFrLr0dJIusd_riUHm5OQj-yq3Ha89UXn7DjQWsvI130_head
{
this:
np:hasAssertion
dgn-np:NP364499.RAophFrLr0dJIusd_riUHm5OQj-yq3Ha89UXn7DjQWsvI130_assertion
;
np:hasProvenance
dgn-np:NP364499.RAophFrLr0dJIusd_riUHm5OQj-yq3Ha89UXn7DjQWsvI130_provenance
;
np:hasPublicationInfo
dgn-np:NP364499.RAophFrLr0dJIusd_riUHm5OQj-yq3Ha89UXn7DjQWsvI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP364499.RAophFrLr0dJIusd_riUHm5OQj-yq3Ha89UXn7DjQWsvI130_assertion
a
np:Assertion
.
dgn-np:NP364499.RAophFrLr0dJIusd_riUHm5OQj-yq3Ha89UXn7DjQWsvI130_provenance
a
np:Provenance
.
dgn-np:NP364499.RAophFrLr0dJIusd_riUHm5OQj-yq3Ha89UXn7DjQWsvI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP364499.RAophFrLr0dJIusd_riUHm5OQj-yq3Ha89UXn7DjQWsvI130_assertion
{
miriam-gene:3126
a
ncit:C16612
.
lld:C0023452
a
ncit:C7057
.
dgn-gda:DGN609830eb3412410bc349613aee6f5805
sio:SIO_000628
miriam-gene:3126
,
lld:C0023452
;
a
sio:SIO_001121
.
}
dgn-np:NP364499.RAophFrLr0dJIusd_riUHm5OQj-yq3Ha89UXn7DjQWsvI130_provenance
{
dgn-np:NP364499.RAophFrLr0dJIusd_riUHm5OQj-yq3Ha89UXn7DjQWsvI130_assertion
dcterms:description
"[A role for specific human leukocyte antigen (HLA) variants in the etiology of childhood acute lymphoblastic leukemia (ALL) has been extensively studied over the last 30 years, but no unambiguous association has been identified.]. 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:21059899
;
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:NP364499.RAophFrLr0dJIusd_riUHm5OQj-yq3Ha89UXn7DjQWsvI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:33+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" .
}