@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP204966.RAVenItlb5skXd3w8gOvBfiTX2xYeliQsetDOymf0lrLw
> .
@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:NP204966.RAVenItlb5skXd3w8gOvBfiTX2xYeliQsetDOymf0lrLw130_head
{
this:
np:hasAssertion
dgn-np:NP204966.RAVenItlb5skXd3w8gOvBfiTX2xYeliQsetDOymf0lrLw130_assertion
;
np:hasProvenance
dgn-np:NP204966.RAVenItlb5skXd3w8gOvBfiTX2xYeliQsetDOymf0lrLw130_provenance
;
np:hasPublicationInfo
dgn-np:NP204966.RAVenItlb5skXd3w8gOvBfiTX2xYeliQsetDOymf0lrLw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP204966.RAVenItlb5skXd3w8gOvBfiTX2xYeliQsetDOymf0lrLw130_assertion
a
np:Assertion
.
dgn-np:NP204966.RAVenItlb5skXd3w8gOvBfiTX2xYeliQsetDOymf0lrLw130_provenance
a
np:Provenance
.
dgn-np:NP204966.RAVenItlb5skXd3w8gOvBfiTX2xYeliQsetDOymf0lrLw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP204966.RAVenItlb5skXd3w8gOvBfiTX2xYeliQsetDOymf0lrLw130_assertion
{
miriam-gene:3702
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN845b4f23461f9224e2faca491e9b1322
sio:SIO_000628
miriam-gene:3702
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP204966.RAVenItlb5skXd3w8gOvBfiTX2xYeliQsetDOymf0lrLw130_provenance
{
dgn-np:NP204966.RAVenItlb5skXd3w8gOvBfiTX2xYeliQsetDOymf0lrLw130_assertion
dcterms:description
"[Taken together, our results demonstrate the roles of multiple microRNAs and p38 signaling in the progression of cancer and demonstrate the therapeutic potential of targeting the p38 MAPK pathway for reversing EMT in an advanced tumor phenotype.]. 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:23403951
;
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:NP204966.RAVenItlb5skXd3w8gOvBfiTX2xYeliQsetDOymf0lrLw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:53+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" .
}