@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP279546.RA5vWyz6LR1BZFSPIk1bKtlcIevA7vj98Fxffp_oGPjVw
> .
@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:NP279546.RA5vWyz6LR1BZFSPIk1bKtlcIevA7vj98Fxffp_oGPjVw130_head
{
this:
np:hasAssertion
dgn-np:NP279546.RA5vWyz6LR1BZFSPIk1bKtlcIevA7vj98Fxffp_oGPjVw130_assertion
;
np:hasProvenance
dgn-np:NP279546.RA5vWyz6LR1BZFSPIk1bKtlcIevA7vj98Fxffp_oGPjVw130_provenance
;
np:hasPublicationInfo
dgn-np:NP279546.RA5vWyz6LR1BZFSPIk1bKtlcIevA7vj98Fxffp_oGPjVw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP279546.RA5vWyz6LR1BZFSPIk1bKtlcIevA7vj98Fxffp_oGPjVw130_assertion
a
np:Assertion
.
dgn-np:NP279546.RA5vWyz6LR1BZFSPIk1bKtlcIevA7vj98Fxffp_oGPjVw130_provenance
a
np:Provenance
.
dgn-np:NP279546.RA5vWyz6LR1BZFSPIk1bKtlcIevA7vj98Fxffp_oGPjVw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP279546.RA5vWyz6LR1BZFSPIk1bKtlcIevA7vj98Fxffp_oGPjVw130_assertion
{
miriam-gene:2120
a
ncit:C16612
.
lld:C0751606
a
ncit:C7057
.
dgn-gda:DGN6097fcf87a0e1d223ee9a034562cdf0c
sio:SIO_000628
miriam-gene:2120
,
lld:C0751606
;
a
sio:SIO_001121
.
}
dgn-np:NP279546.RA5vWyz6LR1BZFSPIk1bKtlcIevA7vj98Fxffp_oGPjVw130_provenance
{
dgn-np:NP279546.RA5vWyz6LR1BZFSPIk1bKtlcIevA7vj98Fxffp_oGPjVw130_assertion
dcterms:description
"[This study shows that multiplex-nested RT-PCR is an effective and accurate tool to identify ETV6 rearrangements in adult ALL, which provides some clues into the diagnosis and prognosis of ALL but also molecular markers for the detection of minimal residual disease in adult 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:22373549
;
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:NP279546.RA5vWyz6LR1BZFSPIk1bKtlcIevA7vj98Fxffp_oGPjVw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:37+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" .
}