@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP188652.RA2zzpkhtiGS-p70xXEyF8iVp0WN7xdXI9yoZcWuL7vgA
> .
@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:NP188652.RA2zzpkhtiGS-p70xXEyF8iVp0WN7xdXI9yoZcWuL7vgA130_head
{
this:
np:hasAssertion
dgn-np:NP188652.RA2zzpkhtiGS-p70xXEyF8iVp0WN7xdXI9yoZcWuL7vgA130_assertion
;
np:hasProvenance
dgn-np:NP188652.RA2zzpkhtiGS-p70xXEyF8iVp0WN7xdXI9yoZcWuL7vgA130_provenance
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np:hasPublicationInfo
dgn-np:NP188652.RA2zzpkhtiGS-p70xXEyF8iVp0WN7xdXI9yoZcWuL7vgA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP188652.RA2zzpkhtiGS-p70xXEyF8iVp0WN7xdXI9yoZcWuL7vgA130_assertion
a
np:Assertion
.
dgn-np:NP188652.RA2zzpkhtiGS-p70xXEyF8iVp0WN7xdXI9yoZcWuL7vgA130_provenance
a
np:Provenance
.
dgn-np:NP188652.RA2zzpkhtiGS-p70xXEyF8iVp0WN7xdXI9yoZcWuL7vgA130_publicationInfo
a
np:PublicationInfo
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}
dgn-np:NP188652.RA2zzpkhtiGS-p70xXEyF8iVp0WN7xdXI9yoZcWuL7vgA130_assertion
{
miriam-gene:611
a
ncit:C16612
.
lld:C0023449
a
ncit:C7057
.
dgn-gda:DGN7dea29036b67b7878335313f674133b9
sio:SIO_000628
miriam-gene:611
,
lld:C0023449
;
a
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.
}
dgn-np:NP188652.RA2zzpkhtiGS-p70xXEyF8iVp0WN7xdXI9yoZcWuL7vgA130_provenance
{
dgn-np:NP188652.RA2zzpkhtiGS-p70xXEyF8iVp0WN7xdXI9yoZcWuL7vgA130_assertion
dcterms:description
"[In this study on 27 t(4;11) infant ALL, we have used standardized primer sets for the detection of all incomplete and complete immunoglobulin (Ig) heavy chain (IGH) rearrangements, as well as for the Ig light chain kappa (IGK), T-cell receptor delta (TCRD) and gamma (TCRG) rearrangements that are most common in childhood BCP 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:11972513
;
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:NP188652.RA2zzpkhtiGS-p70xXEyF8iVp0WN7xdXI9yoZcWuL7vgA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:43+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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pav:authoredBy
<
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> , <
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
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