@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1236788.RAwMqpdMKXAcAONpMrtfWUl92ymW3V6My-g4BkcTJ8prY
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1236788.RAwMqpdMKXAcAONpMrtfWUl92ymW3V6My-g4BkcTJ8prY130_head
{
this:
np:hasAssertion
dgn-np:NP1236788.RAwMqpdMKXAcAONpMrtfWUl92ymW3V6My-g4BkcTJ8prY130_assertion
;
np:hasProvenance
dgn-np:NP1236788.RAwMqpdMKXAcAONpMrtfWUl92ymW3V6My-g4BkcTJ8prY130_provenance
;
np:hasPublicationInfo
dgn-np:NP1236788.RAwMqpdMKXAcAONpMrtfWUl92ymW3V6My-g4BkcTJ8prY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1236788.RAwMqpdMKXAcAONpMrtfWUl92ymW3V6My-g4BkcTJ8prY130_assertion
a
np:Assertion
.
dgn-np:NP1236788.RAwMqpdMKXAcAONpMrtfWUl92ymW3V6My-g4BkcTJ8prY130_provenance
a
np:Provenance
.
dgn-np:NP1236788.RAwMqpdMKXAcAONpMrtfWUl92ymW3V6My-g4BkcTJ8prY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1236788.RAwMqpdMKXAcAONpMrtfWUl92ymW3V6My-g4BkcTJ8prY130_assertion
{
miriam-gene:861
a
ncit:C16612
.
lld:C1961102
a
ncit:C7057
.
dgn-gda:DGNb3c6d5cf2d2b9eeadf61724b77b3a0e6
sio:SIO_000628
miriam-gene:861
,
lld:C1961102
;
a
sio:SIO_001121
.
}
dgn-np:NP1236788.RAwMqpdMKXAcAONpMrtfWUl92ymW3V6My-g4BkcTJ8prY130_provenance
{
dgn-np:NP1236788.RAwMqpdMKXAcAONpMrtfWUl92ymW3V6My-g4BkcTJ8prY130_assertion
dcterms:description
"[We reasoned that shared clonal rearrangements of IG or TCR genes by concordant ALL in twins would be informative about the fetal cell type in which clonal advantage is elicited by ETV6-RUNX1.]. 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:25388957
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1236788.RAwMqpdMKXAcAONpMrtfWUl92ymW3V6My-g4BkcTJ8prY130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:06+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}