@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP472150.RA3fAEI4SwpiHUC6cRxIAhXAtpFSFIGxsTCy8FRnbJiyY
> .
@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:NP472150.RA3fAEI4SwpiHUC6cRxIAhXAtpFSFIGxsTCy8FRnbJiyY130_head
{
this:
np:hasAssertion
dgn-np:NP472150.RA3fAEI4SwpiHUC6cRxIAhXAtpFSFIGxsTCy8FRnbJiyY130_assertion
;
np:hasProvenance
dgn-np:NP472150.RA3fAEI4SwpiHUC6cRxIAhXAtpFSFIGxsTCy8FRnbJiyY130_provenance
;
np:hasPublicationInfo
dgn-np:NP472150.RA3fAEI4SwpiHUC6cRxIAhXAtpFSFIGxsTCy8FRnbJiyY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP472150.RA3fAEI4SwpiHUC6cRxIAhXAtpFSFIGxsTCy8FRnbJiyY130_assertion
a
np:Assertion
.
dgn-np:NP472150.RA3fAEI4SwpiHUC6cRxIAhXAtpFSFIGxsTCy8FRnbJiyY130_provenance
a
np:Provenance
.
dgn-np:NP472150.RA3fAEI4SwpiHUC6cRxIAhXAtpFSFIGxsTCy8FRnbJiyY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP472150.RA3fAEI4SwpiHUC6cRxIAhXAtpFSFIGxsTCy8FRnbJiyY130_assertion
{
miriam-gene:4193
a
ncit:C16612
.
lld:C0023467
a
ncit:C7057
.
dgn-gda:DGN7cc4fe55ed1b95ae5ed1a5ad41dc0289
sio:SIO_000628
miriam-gene:4193
,
lld:C0023467
;
a
sio:SIO_001121
.
}
dgn-np:NP472150.RA3fAEI4SwpiHUC6cRxIAhXAtpFSFIGxsTCy8FRnbJiyY130_provenance
{
dgn-np:NP472150.RA3fAEI4SwpiHUC6cRxIAhXAtpFSFIGxsTCy8FRnbJiyY130_assertion
dcterms:description
"[Although TP53 mutations are rare in acute myeloid leukemia (AML), wild type p53 function is habitually annulled through overexpression of MDM2 or through various mechanisms including epigenetic silencing by histone deacetylases (HDACs).]. 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:22064349
;
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:NP472150.RA3fAEI4SwpiHUC6cRxIAhXAtpFSFIGxsTCy8FRnbJiyY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:43+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" .
}