@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP451916.RAHIS8Z99AqP9dm9AUAjg-z5MVW8vOtHnEMjrJlmAg0UQ
> .
@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:NP451916.RAHIS8Z99AqP9dm9AUAjg-z5MVW8vOtHnEMjrJlmAg0UQ130_head
{
this:
np:hasAssertion
dgn-np:NP451916.RAHIS8Z99AqP9dm9AUAjg-z5MVW8vOtHnEMjrJlmAg0UQ130_assertion
;
np:hasProvenance
dgn-np:NP451916.RAHIS8Z99AqP9dm9AUAjg-z5MVW8vOtHnEMjrJlmAg0UQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP451916.RAHIS8Z99AqP9dm9AUAjg-z5MVW8vOtHnEMjrJlmAg0UQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP451916.RAHIS8Z99AqP9dm9AUAjg-z5MVW8vOtHnEMjrJlmAg0UQ130_assertion
a
np:Assertion
.
dgn-np:NP451916.RAHIS8Z99AqP9dm9AUAjg-z5MVW8vOtHnEMjrJlmAg0UQ130_provenance
a
np:Provenance
.
dgn-np:NP451916.RAHIS8Z99AqP9dm9AUAjg-z5MVW8vOtHnEMjrJlmAg0UQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP451916.RAHIS8Z99AqP9dm9AUAjg-z5MVW8vOtHnEMjrJlmAg0UQ130_assertion
{
miriam-gene:2120
a
ncit:C16612
.
lld:C0376545
a
ncit:C7057
.
dgn-gda:DGNdcceca623542986bcb6ded4d2a5ce6a2
sio:SIO_000628
miriam-gene:2120
,
lld:C0376545
;
a
sio:SIO_001121
.
}
dgn-np:NP451916.RAHIS8Z99AqP9dm9AUAjg-z5MVW8vOtHnEMjrJlmAg0UQ130_provenance
{
dgn-np:NP451916.RAHIS8Z99AqP9dm9AUAjg-z5MVW8vOtHnEMjrJlmAg0UQ130_assertion
dcterms:description
"[Several partner genes on different chromosomes have been reported to be fused with the ETV6 gene (located in chromosome band 12p13), with different breakpoints and different frequencies, in various hematologic malignancies, particularly acute myeloid and lymphoid leukemias and myelodysplastic syndromes.]. 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:9523197
;
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:NP451916.RAHIS8Z99AqP9dm9AUAjg-z5MVW8vOtHnEMjrJlmAg0UQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:29+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" .
}