@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP276041.RAQUwXjLNhEwSBL327sYifa3HAfu1CczsJuFhE69irTGk
> .
@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:NP276041.RAQUwXjLNhEwSBL327sYifa3HAfu1CczsJuFhE69irTGk130_head
{
this:
np:hasAssertion
dgn-np:NP276041.RAQUwXjLNhEwSBL327sYifa3HAfu1CczsJuFhE69irTGk130_assertion
;
np:hasProvenance
dgn-np:NP276041.RAQUwXjLNhEwSBL327sYifa3HAfu1CczsJuFhE69irTGk130_provenance
;
np:hasPublicationInfo
dgn-np:NP276041.RAQUwXjLNhEwSBL327sYifa3HAfu1CczsJuFhE69irTGk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP276041.RAQUwXjLNhEwSBL327sYifa3HAfu1CczsJuFhE69irTGk130_assertion
a
np:Assertion
.
dgn-np:NP276041.RAQUwXjLNhEwSBL327sYifa3HAfu1CczsJuFhE69irTGk130_provenance
a
np:Provenance
.
dgn-np:NP276041.RAQUwXjLNhEwSBL327sYifa3HAfu1CczsJuFhE69irTGk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP276041.RAQUwXjLNhEwSBL327sYifa3HAfu1CczsJuFhE69irTGk130_assertion
{
miriam-gene:23326
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN156febf71d5563a9da6580cc58ab81e2
sio:SIO_000628
miriam-gene:23326
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP276041.RAQUwXjLNhEwSBL327sYifa3HAfu1CczsJuFhE69irTGk130_provenance
{
dgn-np:NP276041.RAQUwXjLNhEwSBL327sYifa3HAfu1CczsJuFhE69irTGk130_assertion
dcterms:description
"[The simultaneous targeting of USP22, and its downstream signal transduction molecules seem highly informative in stratification of the cancer into subgroups with distinct likelihood of therapy failure, which contribute to make decision process regarding the individualized therapy selection and optimization.]. 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:22717106
;
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:NP276041.RAQUwXjLNhEwSBL327sYifa3HAfu1CczsJuFhE69irTGk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:35+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" .
}