@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP615610.RAUvgxvnqL1ipbOT5ReNUbZ8iDjZFc9gzCfPOR5-HxyW4
> .
@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:NP615610.RAUvgxvnqL1ipbOT5ReNUbZ8iDjZFc9gzCfPOR5-HxyW4130_head
{
this:
np:hasAssertion
dgn-np:NP615610.RAUvgxvnqL1ipbOT5ReNUbZ8iDjZFc9gzCfPOR5-HxyW4130_assertion
;
np:hasProvenance
dgn-np:NP615610.RAUvgxvnqL1ipbOT5ReNUbZ8iDjZFc9gzCfPOR5-HxyW4130_provenance
;
np:hasPublicationInfo
dgn-np:NP615610.RAUvgxvnqL1ipbOT5ReNUbZ8iDjZFc9gzCfPOR5-HxyW4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP615610.RAUvgxvnqL1ipbOT5ReNUbZ8iDjZFc9gzCfPOR5-HxyW4130_assertion
a
np:Assertion
.
dgn-np:NP615610.RAUvgxvnqL1ipbOT5ReNUbZ8iDjZFc9gzCfPOR5-HxyW4130_provenance
a
np:Provenance
.
dgn-np:NP615610.RAUvgxvnqL1ipbOT5ReNUbZ8iDjZFc9gzCfPOR5-HxyW4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP615610.RAUvgxvnqL1ipbOT5ReNUbZ8iDjZFc9gzCfPOR5-HxyW4130_assertion
{
miriam-gene:1027
a
ncit:C16612
.
lld:C0007097
a
ncit:C7057
.
dgn-gda:DGN524996c17ce08ea47c9c8fea3bf05aa6
sio:SIO_000628
miriam-gene:1027
,
lld:C0007097
;
a
sio:SIO_001121
.
}
dgn-np:NP615610.RAUvgxvnqL1ipbOT5ReNUbZ8iDjZFc9gzCfPOR5-HxyW4130_provenance
{
dgn-np:NP615610.RAUvgxvnqL1ipbOT5ReNUbZ8iDjZFc9gzCfPOR5-HxyW4130_assertion
dcterms:description
"[Those results suggest that (a) overexpression of Skp2 through an amplification mechanism may contribute to the progression of BTC, (b) not only each molecule, but also the combination of Skp2 and p27Kip1, might be a useful predictor of the prognosis of BTC, and (c) molecular targets of Skp2 other than p27Kip1 may also be important factors in the pathogenesis of this disease.]. 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:15596046
;
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:NP615610.RAUvgxvnqL1ipbOT5ReNUbZ8iDjZFc9gzCfPOR5-HxyW4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:12+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" .
}