@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP796471.RAPpGMItmuKqTprifHdiOXx06DaWKtWdtY16uBa3JDHew
> .
@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:NP796471.RAPpGMItmuKqTprifHdiOXx06DaWKtWdtY16uBa3JDHew130_head
{
this:
np:hasAssertion
dgn-np:NP796471.RAPpGMItmuKqTprifHdiOXx06DaWKtWdtY16uBa3JDHew130_assertion
;
np:hasProvenance
dgn-np:NP796471.RAPpGMItmuKqTprifHdiOXx06DaWKtWdtY16uBa3JDHew130_provenance
;
np:hasPublicationInfo
dgn-np:NP796471.RAPpGMItmuKqTprifHdiOXx06DaWKtWdtY16uBa3JDHew130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP796471.RAPpGMItmuKqTprifHdiOXx06DaWKtWdtY16uBa3JDHew130_assertion
a
np:Assertion
.
dgn-np:NP796471.RAPpGMItmuKqTprifHdiOXx06DaWKtWdtY16uBa3JDHew130_provenance
a
np:Provenance
.
dgn-np:NP796471.RAPpGMItmuKqTprifHdiOXx06DaWKtWdtY16uBa3JDHew130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP796471.RAPpGMItmuKqTprifHdiOXx06DaWKtWdtY16uBa3JDHew130_assertion
{
miriam-gene:3662
a
ncit:C16612
.
lld:C0023473
a
ncit:C7057
.
dgn-gda:DGN4d98d6c3f1f0d2d326ee5a54c0b7d535
sio:SIO_000628
miriam-gene:3662
,
lld:C0023473
;
a
sio:SIO_001121
.
}
dgn-np:NP796471.RAPpGMItmuKqTprifHdiOXx06DaWKtWdtY16uBa3JDHew130_provenance
{
dgn-np:NP796471.RAPpGMItmuKqTprifHdiOXx06DaWKtWdtY16uBa3JDHew130_assertion
dcterms:description
"[Although the bcr-abl translocation has been shown to be the causative genetic aberration in chronic myeloid leukemia (CML), there is mounting evidence that the deregulation of other genes, such as the transcription factor interferon regulatory factor 4 (IRF-4), is also implicated in the pathogenesis of CML.]. 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:16396836
;
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:NP796471.RAPpGMItmuKqTprifHdiOXx06DaWKtWdtY16uBa3JDHew130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:09+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" .
}