@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1351046.RAQLqpAlWmCCEoID7RoJTVb-ddVUEFjfPiKOuDArvwtVg
> .
@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/v4.0.0/void/
> .
dgn-np:NP1351046.RAQLqpAlWmCCEoID7RoJTVb-ddVUEFjfPiKOuDArvwtVg130_head
{
this:
np:hasAssertion
dgn-np:NP1351046.RAQLqpAlWmCCEoID7RoJTVb-ddVUEFjfPiKOuDArvwtVg130_assertion
;
np:hasProvenance
dgn-np:NP1351046.RAQLqpAlWmCCEoID7RoJTVb-ddVUEFjfPiKOuDArvwtVg130_provenance
;
np:hasPublicationInfo
dgn-np:NP1351046.RAQLqpAlWmCCEoID7RoJTVb-ddVUEFjfPiKOuDArvwtVg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1351046.RAQLqpAlWmCCEoID7RoJTVb-ddVUEFjfPiKOuDArvwtVg130_assertion
a
np:Assertion
.
dgn-np:NP1351046.RAQLqpAlWmCCEoID7RoJTVb-ddVUEFjfPiKOuDArvwtVg130_provenance
a
np:Provenance
.
dgn-np:NP1351046.RAQLqpAlWmCCEoID7RoJTVb-ddVUEFjfPiKOuDArvwtVg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1351046.RAQLqpAlWmCCEoID7RoJTVb-ddVUEFjfPiKOuDArvwtVg130_assertion
{
miriam-gene:2078
a
ncit:C16612
.
lld:C0553580
a
ncit:C7057
.
dgn-gda:DGN3601dbd7b5d72b8a18d3e1601c27ef45
sio:SIO_000628
miriam-gene:2078
,
lld:C0553580
;
a
sio:SIO_001121
.
}
dgn-np:NP1351046.RAQLqpAlWmCCEoID7RoJTVb-ddVUEFjfPiKOuDArvwtVg130_provenance
{
dgn-np:NP1351046.RAQLqpAlWmCCEoID7RoJTVb-ddVUEFjfPiKOuDArvwtVg130_assertion
dcterms:description
"[Because of the high heterogeneity of EWS gene fusions with FLI1 and ERG genes due to variable chromosomal breakpoint locations in Ewing tumors (ET) (14 different chimeric transcripts identified so far), we evaluated the clinical impact of the expression of diverse fusion transcripts in ET patients.]. 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:8648380
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1351046.RAQLqpAlWmCCEoID7RoJTVb-ddVUEFjfPiKOuDArvwtVg130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:58+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}