@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP473489.RADJI4Ho_mNpnZWptOygAG6F65vjnXEoUBrhWK8CcCXho
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP473489.RADJI4Ho_mNpnZWptOygAG6F65vjnXEoUBrhWK8CcCXho130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP473489.RADJI4Ho_mNpnZWptOygAG6F65vjnXEoUBrhWK8CcCXho130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP473489.RADJI4Ho_mNpnZWptOygAG6F65vjnXEoUBrhWK8CcCXho130_assertion
a
np:Assertion
.
dgn-np:NP473489.RADJI4Ho_mNpnZWptOygAG6F65vjnXEoUBrhWK8CcCXho130_provenance
a
np:Provenance
.
dgn-np:NP473489.RADJI4Ho_mNpnZWptOygAG6F65vjnXEoUBrhWK8CcCXho130_publicationInfo
a
np:PublicationInfo
.
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dgn-np:NP473489.RADJI4Ho_mNpnZWptOygAG6F65vjnXEoUBrhWK8CcCXho130_assertion
{
miriam-gene:2115
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN8b1b57398d48fb10f4169ee5ec72b309
sio:SIO_000628
miriam-gene:2115
,
lld:C0006826
;
a
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.
}
dgn-np:NP473489.RADJI4Ho_mNpnZWptOygAG6F65vjnXEoUBrhWK8CcCXho130_provenance
{
dgn-np:NP473489.RADJI4Ho_mNpnZWptOygAG6F65vjnXEoUBrhWK8CcCXho130_assertion
dcterms:description
"[The findings of the present study give further mechanistic insights into why ETV1 is highly expressed in certain cancers, indicate that loss of capicúa can desensitize cells to the effects of ERK pathway inhibitors, and highlight interconnections among growth factor signalling, spinocerebellar ataxias and cancers.]. 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:21087211
;
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:NP473489.RADJI4Ho_mNpnZWptOygAG6F65vjnXEoUBrhWK8CcCXho130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:43+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
<
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> , <
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> , <
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> , <
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> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
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