@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1284826.RAlXf-p-vOOhzSCWCMm2hqL85jxNzTLUIFLxw65DZ4dfY
> .
@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:NP1284826.RAlXf-p-vOOhzSCWCMm2hqL85jxNzTLUIFLxw65DZ4dfY130_head
{
this:
np:hasAssertion
dgn-np:NP1284826.RAlXf-p-vOOhzSCWCMm2hqL85jxNzTLUIFLxw65DZ4dfY130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
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a
np:Nanopublication
.
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a
np:Assertion
.
dgn-np:NP1284826.RAlXf-p-vOOhzSCWCMm2hqL85jxNzTLUIFLxw65DZ4dfY130_provenance
a
np:Provenance
.
dgn-np:NP1284826.RAlXf-p-vOOhzSCWCMm2hqL85jxNzTLUIFLxw65DZ4dfY130_publicationInfo
a
np:PublicationInfo
.
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{
miriam-gene:3172
a
ncit:C16612
.
lld:C0400966
a
ncit:C7057
.
dgn-gda:DGNf1228d0c896dc37d4f77e5c3b98dd405
sio:SIO_000628
miriam-gene:3172
,
lld:C0400966
;
a
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.
}
dgn-np:NP1284826.RAlXf-p-vOOhzSCWCMm2hqL85jxNzTLUIFLxw65DZ4dfY130_provenance
{
dgn-np:NP1284826.RAlXf-p-vOOhzSCWCMm2hqL85jxNzTLUIFLxw65DZ4dfY130_assertion
dcterms:description
"[Our findings show that: (I) HNF4 is a common potential transcription factor mediating the transcription of NAFLD progression genes (II) mice HCC derived from NAFLD co-cluster with a less aggressive human HCC subtype of differential prognosis and mixed etiology (III) the HCC survival signature is able to correctly classify 95% of the samples and gives Fgf20 and Tgfb1i1 as the most robust genes for prediction (IV) the expression values of genes composing the signature in an independent human HCC dataset revealed different HCC subtypes showing differences in survival time by a Logrank test.]. 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:25993042
;
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:NP1284826.RAlXf-p-vOOhzSCWCMm2hqL85jxNzTLUIFLxw65DZ4dfY130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:28+02:00"^^
xsd:dateTime
;
dcterms:rights
<
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> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
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;
pav:authoredBy
<
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> , <
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http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
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> ;
pav:version
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dgn-void:disgenetv3.0rdf
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"v4.0.0" .
}