@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP814143.RAkcYBMwhr0Pr90O6V69cWVofe0f4v8nJciw6lvHQ-bzU
> .
@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:NP814143.RAkcYBMwhr0Pr90O6V69cWVofe0f4v8nJciw6lvHQ-bzU130_head
{
this:
np:hasAssertion
dgn-np:NP814143.RAkcYBMwhr0Pr90O6V69cWVofe0f4v8nJciw6lvHQ-bzU130_assertion
;
np:hasProvenance
dgn-np:NP814143.RAkcYBMwhr0Pr90O6V69cWVofe0f4v8nJciw6lvHQ-bzU130_provenance
;
np:hasPublicationInfo
dgn-np:NP814143.RAkcYBMwhr0Pr90O6V69cWVofe0f4v8nJciw6lvHQ-bzU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP814143.RAkcYBMwhr0Pr90O6V69cWVofe0f4v8nJciw6lvHQ-bzU130_assertion
a
np:Assertion
.
dgn-np:NP814143.RAkcYBMwhr0Pr90O6V69cWVofe0f4v8nJciw6lvHQ-bzU130_provenance
a
np:Provenance
.
dgn-np:NP814143.RAkcYBMwhr0Pr90O6V69cWVofe0f4v8nJciw6lvHQ-bzU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP814143.RAkcYBMwhr0Pr90O6V69cWVofe0f4v8nJciw6lvHQ-bzU130_assertion
{
miriam-gene:2130
a
ncit:C16612
.
lld:C0796070
a
ncit:C7057
.
dgn-gda:DGNbce1e845ea72813dbe6fbb7a7aef948e
sio:SIO_000628
miriam-gene:2130
,
lld:C0796070
;
a
sio:SIO_001121
.
}
dgn-np:NP814143.RAkcYBMwhr0Pr90O6V69cWVofe0f4v8nJciw6lvHQ-bzU130_provenance
{
dgn-np:NP814143.RAkcYBMwhr0Pr90O6V69cWVofe0f4v8nJciw6lvHQ-bzU130_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 .
}
dgn-np:NP814143.RAkcYBMwhr0Pr90O6V69cWVofe0f4v8nJciw6lvHQ-bzU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:19+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" .
}