@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP508098.RAgvSpf_Ce2g85Rw479yZbxqaJ25wfZt2TtvV3Y4kz2YI
> .
@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:NP508098.RAgvSpf_Ce2g85Rw479yZbxqaJ25wfZt2TtvV3Y4kz2YI130_head
{
this:
np:hasAssertion
dgn-np:NP508098.RAgvSpf_Ce2g85Rw479yZbxqaJ25wfZt2TtvV3Y4kz2YI130_assertion
;
np:hasProvenance
dgn-np:NP508098.RAgvSpf_Ce2g85Rw479yZbxqaJ25wfZt2TtvV3Y4kz2YI130_provenance
;
np:hasPublicationInfo
dgn-np:NP508098.RAgvSpf_Ce2g85Rw479yZbxqaJ25wfZt2TtvV3Y4kz2YI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP508098.RAgvSpf_Ce2g85Rw479yZbxqaJ25wfZt2TtvV3Y4kz2YI130_assertion
a
np:Assertion
.
dgn-np:NP508098.RAgvSpf_Ce2g85Rw479yZbxqaJ25wfZt2TtvV3Y4kz2YI130_provenance
a
np:Provenance
.
dgn-np:NP508098.RAgvSpf_Ce2g85Rw479yZbxqaJ25wfZt2TtvV3Y4kz2YI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP508098.RAgvSpf_Ce2g85Rw479yZbxqaJ25wfZt2TtvV3Y4kz2YI130_assertion
{
miriam-gene:4594
a
ncit:C16612
.
lld:C0376358
a
ncit:C7057
.
dgn-gda:DGN0ffa4ffdb2153a72551822b4b9215d87
sio:SIO_000628
miriam-gene:4594
,
lld:C0376358
;
a
sio:SIO_001121
.
}
dgn-np:NP508098.RAgvSpf_Ce2g85Rw479yZbxqaJ25wfZt2TtvV3Y4kz2YI130_provenance
{
dgn-np:NP508098.RAgvSpf_Ce2g85Rw479yZbxqaJ25wfZt2TtvV3Y4kz2YI130_assertion
dcterms:description
"[Taken together, our data show that induction of MEK5/ERK5 signalling is linked to activation of the DNA replication licensing pathway in PCa, and that the strong prognostic value of MCM proteins may result from their function as relay stations coupling growth regulatory pathways to genome duplication.]. 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:17406359
;
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:NP508098.RAgvSpf_Ce2g85Rw479yZbxqaJ25wfZt2TtvV3Y4kz2YI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:03+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" .
}