@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP471197.RACGYb65LcNX2wzvzxXtkBi26gi24iO4ftwMSod9zXmFI
> .
@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:NP471197.RACGYb65LcNX2wzvzxXtkBi26gi24iO4ftwMSod9zXmFI130_head
{
this:
np:hasAssertion
dgn-np:NP471197.RACGYb65LcNX2wzvzxXtkBi26gi24iO4ftwMSod9zXmFI130_assertion
;
np:hasProvenance
dgn-np:NP471197.RACGYb65LcNX2wzvzxXtkBi26gi24iO4ftwMSod9zXmFI130_provenance
;
np:hasPublicationInfo
dgn-np:NP471197.RACGYb65LcNX2wzvzxXtkBi26gi24iO4ftwMSod9zXmFI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP471197.RACGYb65LcNX2wzvzxXtkBi26gi24iO4ftwMSod9zXmFI130_assertion
a
np:Assertion
.
dgn-np:NP471197.RACGYb65LcNX2wzvzxXtkBi26gi24iO4ftwMSod9zXmFI130_provenance
a
np:Provenance
.
dgn-np:NP471197.RACGYb65LcNX2wzvzxXtkBi26gi24iO4ftwMSod9zXmFI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP471197.RACGYb65LcNX2wzvzxXtkBi26gi24iO4ftwMSod9zXmFI130_assertion
{
miriam-gene:5715
a
ncit:C16612
.
lld:C0027651
a
ncit:C7057
.
dgn-gda:DGN28602d34a490a98c3c31d97d2158d682
sio:SIO_000628
miriam-gene:5715
,
lld:C0027651
;
a
sio:SIO_001121
.
}
dgn-np:NP471197.RACGYb65LcNX2wzvzxXtkBi26gi24iO4ftwMSod9zXmFI130_provenance
{
dgn-np:NP471197.RACGYb65LcNX2wzvzxXtkBi26gi24iO4ftwMSod9zXmFI130_assertion
dcterms:description
"[We conclude that in solid pseudopapillary neoplasms the activated Wnt-signaling pathway is disrupted, and that p21 and p27 are contributing to this fact by blocking of the hyperphosphorylation of the Rb protein, thus causing the very low proliferation rate characterizing the solid pseudopapillary neoplasms.]. 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:17632456
;
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:NP471197.RACGYb65LcNX2wzvzxXtkBi26gi24iO4ftwMSod9zXmFI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:42+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" .
}