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http://rdf.disgenet.org/nanopublications.trig#NP568760.RA9mHMytqiciaSUT53IUdg2XwmmxgILydHz2dTyJySfRA
> .
@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:NP568760.RA9mHMytqiciaSUT53IUdg2XwmmxgILydHz2dTyJySfRA130_head
{
this:
np:hasAssertion
dgn-np:NP568760.RA9mHMytqiciaSUT53IUdg2XwmmxgILydHz2dTyJySfRA130_assertion
;
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;
np:hasPublicationInfo
dgn-np:NP568760.RA9mHMytqiciaSUT53IUdg2XwmmxgILydHz2dTyJySfRA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP568760.RA9mHMytqiciaSUT53IUdg2XwmmxgILydHz2dTyJySfRA130_assertion
a
np:Assertion
.
dgn-np:NP568760.RA9mHMytqiciaSUT53IUdg2XwmmxgILydHz2dTyJySfRA130_provenance
a
np:Provenance
.
dgn-np:NP568760.RA9mHMytqiciaSUT53IUdg2XwmmxgILydHz2dTyJySfRA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP568760.RA9mHMytqiciaSUT53IUdg2XwmmxgILydHz2dTyJySfRA130_assertion
{
miriam-gene:2521
a
ncit:C16612
.
lld:C0796070
a
ncit:C7057
.
dgn-gda:DGN7399ec9e5a367f058e1dd2949ca03ed2
sio:SIO_000628
miriam-gene:2521
,
lld:C0796070
;
a
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.
}
dgn-np:NP568760.RA9mHMytqiciaSUT53IUdg2XwmmxgILydHz2dTyJySfRA130_provenance
{
dgn-np:NP568760.RA9mHMytqiciaSUT53IUdg2XwmmxgILydHz2dTyJySfRA130_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-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 .
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dgn-np:NP568760.RA9mHMytqiciaSUT53IUdg2XwmmxgILydHz2dTyJySfRA130_publicationInfo
{
this:
dcterms:created
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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
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pav:authoredBy
<
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> , <
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> , <
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
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"v2.1.0" .
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