@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP690020.RAwJ0_23hgPHRNJjlhZaJTTiRgF3XU5sxGFAWf_4TVpA0
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP690020.RAwJ0_23hgPHRNJjlhZaJTTiRgF3XU5sxGFAWf_4TVpA0130_head
{
this:
np:hasAssertion
dgn-np:NP690020.RAwJ0_23hgPHRNJjlhZaJTTiRgF3XU5sxGFAWf_4TVpA0130_assertion
;
np:hasProvenance
dgn-np:NP690020.RAwJ0_23hgPHRNJjlhZaJTTiRgF3XU5sxGFAWf_4TVpA0130_provenance
;
np:hasPublicationInfo
dgn-np:NP690020.RAwJ0_23hgPHRNJjlhZaJTTiRgF3XU5sxGFAWf_4TVpA0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP690020.RAwJ0_23hgPHRNJjlhZaJTTiRgF3XU5sxGFAWf_4TVpA0130_assertion
a
np:Assertion
.
dgn-np:NP690020.RAwJ0_23hgPHRNJjlhZaJTTiRgF3XU5sxGFAWf_4TVpA0130_provenance
a
np:Provenance
.
dgn-np:NP690020.RAwJ0_23hgPHRNJjlhZaJTTiRgF3XU5sxGFAWf_4TVpA0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP690020.RAwJ0_23hgPHRNJjlhZaJTTiRgF3XU5sxGFAWf_4TVpA0130_assertion
{
miriam-gene:1649
a
ncit:C16612
.
lld:C0206634
a
ncit:C7057
.
dgn-gda:DGN6d3ede8e6edd206f0d0db47218d7e768
sio:SIO_000628
miriam-gene:1649
,
lld:C0206634
;
a
sio:SIO_001121
.
}
dgn-np:NP690020.RAwJ0_23hgPHRNJjlhZaJTTiRgF3XU5sxGFAWf_4TVpA0130_provenance
{
dgn-np:NP690020.RAwJ0_23hgPHRNJjlhZaJTTiRgF3XU5sxGFAWf_4TVpA0130_assertion
dcterms:description
"[Our results suggest that characteristic sequence motifs located at the FUS, EWS and CHOP breakpoint regions, including Alu and palindromic oligomer sequences, are involved in the mechanisms creating chromosomal translocations in MLS.]. 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:18752119
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP690020.RAwJ0_23hgPHRNJjlhZaJTTiRgF3XU5sxGFAWf_4TVpA0130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:58+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}