@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP550626.RAPjCEBXMWXUWv8d-13ncjYWcCmhnqddIO9L_AC_Xi8vs
> .
@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:NP550626.RAPjCEBXMWXUWv8d-13ncjYWcCmhnqddIO9L_AC_Xi8vs130_head
{
this:
np:hasAssertion
dgn-np:NP550626.RAPjCEBXMWXUWv8d-13ncjYWcCmhnqddIO9L_AC_Xi8vs130_assertion
;
np:hasProvenance
dgn-np:NP550626.RAPjCEBXMWXUWv8d-13ncjYWcCmhnqddIO9L_AC_Xi8vs130_provenance
;
np:hasPublicationInfo
dgn-np:NP550626.RAPjCEBXMWXUWv8d-13ncjYWcCmhnqddIO9L_AC_Xi8vs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP550626.RAPjCEBXMWXUWv8d-13ncjYWcCmhnqddIO9L_AC_Xi8vs130_assertion
a
np:Assertion
.
dgn-np:NP550626.RAPjCEBXMWXUWv8d-13ncjYWcCmhnqddIO9L_AC_Xi8vs130_provenance
a
np:Provenance
.
dgn-np:NP550626.RAPjCEBXMWXUWv8d-13ncjYWcCmhnqddIO9L_AC_Xi8vs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP550626.RAPjCEBXMWXUWv8d-13ncjYWcCmhnqddIO9L_AC_Xi8vs130_assertion
{
miriam-gene:2130
a
ncit:C16612
.
lld:C0022665
a
ncit:C7057
.
dgn-gda:DGNc585be5d832d6bb7e666c0a0006d242f
sio:SIO_000628
miriam-gene:2130
,
lld:C0022665
;
a
sio:SIO_001121
.
}
dgn-np:NP550626.RAPjCEBXMWXUWv8d-13ncjYWcCmhnqddIO9L_AC_Xi8vs130_provenance
{
dgn-np:NP550626.RAPjCEBXMWXUWv8d-13ncjYWcCmhnqddIO9L_AC_Xi8vs130_assertion
dcterms:description
"[As EWSR1 rearrangements are known to be a characteristic of Ewing tumors (ET), our findings illustrate the diagnostic problems regarding small cell kidney tumors and strongly argue for the need of adjuvant diagnostic techniques in this group of neoplasms.]. 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:18615675
;
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:NP550626.RAPjCEBXMWXUWv8d-13ncjYWcCmhnqddIO9L_AC_Xi8vs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:32+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" .
}