@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP893408.RAncCjWe7eLksSwimuewUfplNHyyMTRdRtqt1qCi193uQ
> .
@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:NP893408.RAncCjWe7eLksSwimuewUfplNHyyMTRdRtqt1qCi193uQ130_head
{
this:
np:hasAssertion
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;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP893408.RAncCjWe7eLksSwimuewUfplNHyyMTRdRtqt1qCi193uQ130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP893408.RAncCjWe7eLksSwimuewUfplNHyyMTRdRtqt1qCi193uQ130_assertion
a
np:Assertion
.
dgn-np:NP893408.RAncCjWe7eLksSwimuewUfplNHyyMTRdRtqt1qCi193uQ130_provenance
a
np:Provenance
.
dgn-np:NP893408.RAncCjWe7eLksSwimuewUfplNHyyMTRdRtqt1qCi193uQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP893408.RAncCjWe7eLksSwimuewUfplNHyyMTRdRtqt1qCi193uQ130_assertion
{
miriam-gene:8815
a
ncit:C16612
.
lld:C0039101
a
ncit:C7057
.
dgn-gda:DGN81d671662a4bfb987817c411aa11c3db
sio:SIO_000628
miriam-gene:8815
,
lld:C0039101
;
a
sio:SIO_001121
.
}
dgn-np:NP893408.RAncCjWe7eLksSwimuewUfplNHyyMTRdRtqt1qCi193uQ130_provenance
{
dgn-np:NP893408.RAncCjWe7eLksSwimuewUfplNHyyMTRdRtqt1qCi193uQ130_assertion
dcterms:description
"[To investigate the underlying mechanism, we studied human synovial sarcoma (SS), in which transformation results from the translocation of exactly 78 amino acids of SSX to the SS18 subunit of BAF complexes.]. 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:23540691
;
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:NP893408.RAncCjWe7eLksSwimuewUfplNHyyMTRdRtqt1qCi193uQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:09+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
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pav:authoredBy
<
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> , <
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> , <
http://orcid.org/0000-0002-9383-528X
> , <
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> , <
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
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"v2.1.0" .
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