@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP387972.RAJ2tscZPoj5OleghUMSM8qssLbo4C0FPT5OSDDP8aXKU
> .
@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/v3.0.0/void/
> .
dgn-np:NP387972.RAJ2tscZPoj5OleghUMSM8qssLbo4C0FPT5OSDDP8aXKU130_head
{
this:
np:hasAssertion
dgn-np:NP387972.RAJ2tscZPoj5OleghUMSM8qssLbo4C0FPT5OSDDP8aXKU130_assertion
;
np:hasProvenance
dgn-np:NP387972.RAJ2tscZPoj5OleghUMSM8qssLbo4C0FPT5OSDDP8aXKU130_provenance
;
np:hasPublicationInfo
dgn-np:NP387972.RAJ2tscZPoj5OleghUMSM8qssLbo4C0FPT5OSDDP8aXKU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP387972.RAJ2tscZPoj5OleghUMSM8qssLbo4C0FPT5OSDDP8aXKU130_assertion
a
np:Assertion
.
dgn-np:NP387972.RAJ2tscZPoj5OleghUMSM8qssLbo4C0FPT5OSDDP8aXKU130_provenance
a
np:Provenance
.
dgn-np:NP387972.RAJ2tscZPoj5OleghUMSM8qssLbo4C0FPT5OSDDP8aXKU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP387972.RAJ2tscZPoj5OleghUMSM8qssLbo4C0FPT5OSDDP8aXKU130_assertion
{
miriam-gene:2130
a
ncit:C16612
.
lld:C0206634
a
ncit:C7057
.
dgn-gda:DGN5d18ec244b72a9a770ee71cbf7a1ffe5
sio:SIO_000628
miriam-gene:2130
,
lld:C0206634
;
a
sio:SIO_001121
.
}
dgn-np:NP387972.RAJ2tscZPoj5OleghUMSM8qssLbo4C0FPT5OSDDP8aXKU130_provenance
{
dgn-np:NP387972.RAJ2tscZPoj5OleghUMSM8qssLbo4C0FPT5OSDDP8aXKU130_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-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP387972.RAJ2tscZPoj5OleghUMSM8qssLbo4C0FPT5OSDDP8aXKU130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:41:24+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}