@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP644525.RArbY6H3UzhlNIKX2qTbinWr5lbJfb81paKpUylzC7PJg
> .
@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:NP644525.RArbY6H3UzhlNIKX2qTbinWr5lbJfb81paKpUylzC7PJg130_head
{
this:
np:hasAssertion
dgn-np:NP644525.RArbY6H3UzhlNIKX2qTbinWr5lbJfb81paKpUylzC7PJg130_assertion
;
np:hasProvenance
dgn-np:NP644525.RArbY6H3UzhlNIKX2qTbinWr5lbJfb81paKpUylzC7PJg130_provenance
;
np:hasPublicationInfo
dgn-np:NP644525.RArbY6H3UzhlNIKX2qTbinWr5lbJfb81paKpUylzC7PJg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP644525.RArbY6H3UzhlNIKX2qTbinWr5lbJfb81paKpUylzC7PJg130_assertion
a
np:Assertion
.
dgn-np:NP644525.RArbY6H3UzhlNIKX2qTbinWr5lbJfb81paKpUylzC7PJg130_provenance
a
np:Provenance
.
dgn-np:NP644525.RArbY6H3UzhlNIKX2qTbinWr5lbJfb81paKpUylzC7PJg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP644525.RArbY6H3UzhlNIKX2qTbinWr5lbJfb81paKpUylzC7PJg130_assertion
{
miriam-gene:6965
a
ncit:C16612
.
lld:C0023452
a
ncit:C7057
.
dgn-gda:DGN0c09422b551c5f68337c33208c47e5c6
sio:SIO_000628
miriam-gene:6965
,
lld:C0023452
;
a
sio:SIO_001121
.
}
dgn-np:NP644525.RArbY6H3UzhlNIKX2qTbinWr5lbJfb81paKpUylzC7PJg130_provenance
{
dgn-np:NP644525.RArbY6H3UzhlNIKX2qTbinWr5lbJfb81paKpUylzC7PJg130_assertion
dcterms:description
"[The high frequency of T cell receptor gamma (TCRG) gene rearrangements in both B-lineage and T cell acute lymphoblastic leukemia (ALL), its easy detection and the lower incidence of oligoclonality make this gene one of the main target for the detection of minimal residual disease by PCR in 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:14687622
;
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:NP644525.RArbY6H3UzhlNIKX2qTbinWr5lbJfb81paKpUylzC7PJg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:28+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" .
}