@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP730778.RAbcf1DAn7GTbpwHRDIN6hn29W9JTHpWlJEbuNvyAAsXE
> .
@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:NP730778.RAbcf1DAn7GTbpwHRDIN6hn29W9JTHpWlJEbuNvyAAsXE130_head
{
this:
np:hasAssertion
dgn-np:NP730778.RAbcf1DAn7GTbpwHRDIN6hn29W9JTHpWlJEbuNvyAAsXE130_assertion
;
np:hasProvenance
dgn-np:NP730778.RAbcf1DAn7GTbpwHRDIN6hn29W9JTHpWlJEbuNvyAAsXE130_provenance
;
np:hasPublicationInfo
dgn-np:NP730778.RAbcf1DAn7GTbpwHRDIN6hn29W9JTHpWlJEbuNvyAAsXE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP730778.RAbcf1DAn7GTbpwHRDIN6hn29W9JTHpWlJEbuNvyAAsXE130_assertion
a
np:Assertion
.
dgn-np:NP730778.RAbcf1DAn7GTbpwHRDIN6hn29W9JTHpWlJEbuNvyAAsXE130_provenance
a
np:Provenance
.
dgn-np:NP730778.RAbcf1DAn7GTbpwHRDIN6hn29W9JTHpWlJEbuNvyAAsXE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP730778.RAbcf1DAn7GTbpwHRDIN6hn29W9JTHpWlJEbuNvyAAsXE130_assertion
{
miriam-gene:6774
a
ncit:C16612
.
lld:C0553580
a
ncit:C7057
.
dgn-gda:DGNa5b5a95f9c63d102ab5361de85b039d8
sio:SIO_000628
miriam-gene:6774
,
lld:C0553580
;
a
sio:SIO_001121
.
}
dgn-np:NP730778.RAbcf1DAn7GTbpwHRDIN6hn29W9JTHpWlJEbuNvyAAsXE130_provenance
{
dgn-np:NP730778.RAbcf1DAn7GTbpwHRDIN6hn29W9JTHpWlJEbuNvyAAsXE130_assertion
dcterms:description
"[In this study, STAT3 activation was assessed in the Ewing sarcoma family of tumours (ESFT), which is characterized by fusion of the EWS gene with one of several Ets transcription factors, most commonly EWS-FLI1.]. 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:16463269
;
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:NP730778.RAbcf1DAn7GTbpwHRDIN6hn29W9JTHpWlJEbuNvyAAsXE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:23+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" .
}