@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP244896.RAdYN4wwDBTwlFbCdWvYXAEwqDT-aeWkJtXxgB_OZ9m1Q
> .
@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:NP244896.RAdYN4wwDBTwlFbCdWvYXAEwqDT-aeWkJtXxgB_OZ9m1Q130_head
{
this:
np:hasAssertion
dgn-np:NP244896.RAdYN4wwDBTwlFbCdWvYXAEwqDT-aeWkJtXxgB_OZ9m1Q130_assertion
;
np:hasProvenance
dgn-np:NP244896.RAdYN4wwDBTwlFbCdWvYXAEwqDT-aeWkJtXxgB_OZ9m1Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP244896.RAdYN4wwDBTwlFbCdWvYXAEwqDT-aeWkJtXxgB_OZ9m1Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP244896.RAdYN4wwDBTwlFbCdWvYXAEwqDT-aeWkJtXxgB_OZ9m1Q130_assertion
a
np:Assertion
.
dgn-np:NP244896.RAdYN4wwDBTwlFbCdWvYXAEwqDT-aeWkJtXxgB_OZ9m1Q130_provenance
a
np:Provenance
.
dgn-np:NP244896.RAdYN4wwDBTwlFbCdWvYXAEwqDT-aeWkJtXxgB_OZ9m1Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP244896.RAdYN4wwDBTwlFbCdWvYXAEwqDT-aeWkJtXxgB_OZ9m1Q130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0007134
a
ncit:C7057
.
dgn-gda:DGNacae9fd28f6e2a9e33b412ef743923c1
sio:SIO_000628
miriam-gene:7157
,
lld:C0007134
;
a
sio:SIO_001121
.
}
dgn-np:NP244896.RAdYN4wwDBTwlFbCdWvYXAEwqDT-aeWkJtXxgB_OZ9m1Q130_provenance
{
dgn-np:NP244896.RAdYN4wwDBTwlFbCdWvYXAEwqDT-aeWkJtXxgB_OZ9m1Q130_assertion
dcterms:description
"[MDM2 expression, combined with increased p53 expression, is associated with reduced survival in several cancers, but is particularly of interest in renal cell carcinoma (RCC) where evidence suggests the presence of tissue-specific p53/MDM2 pathway defects.]. 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:21504894
;
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:NP244896.RAdYN4wwDBTwlFbCdWvYXAEwqDT-aeWkJtXxgB_OZ9m1Q130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:17+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" .
}