@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP563964.RA-B_MM97Nixngyj4Yo8NkmiS_Oc4H44S3MTlZQZUaGK4
> .
@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:NP563964.RA-B_MM97Nixngyj4Yo8NkmiS_Oc4H44S3MTlZQZUaGK4130_head
{
this:
np:hasAssertion
dgn-np:NP563964.RA-B_MM97Nixngyj4Yo8NkmiS_Oc4H44S3MTlZQZUaGK4130_assertion
;
np:hasProvenance
dgn-np:NP563964.RA-B_MM97Nixngyj4Yo8NkmiS_Oc4H44S3MTlZQZUaGK4130_provenance
;
np:hasPublicationInfo
dgn-np:NP563964.RA-B_MM97Nixngyj4Yo8NkmiS_Oc4H44S3MTlZQZUaGK4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP563964.RA-B_MM97Nixngyj4Yo8NkmiS_Oc4H44S3MTlZQZUaGK4130_assertion
a
np:Assertion
.
dgn-np:NP563964.RA-B_MM97Nixngyj4Yo8NkmiS_Oc4H44S3MTlZQZUaGK4130_provenance
a
np:Provenance
.
dgn-np:NP563964.RA-B_MM97Nixngyj4Yo8NkmiS_Oc4H44S3MTlZQZUaGK4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP563964.RA-B_MM97Nixngyj4Yo8NkmiS_Oc4H44S3MTlZQZUaGK4130_assertion
{
miriam-gene:50484
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN43759d19158f32757323d1b4e18109c1
sio:SIO_000628
miriam-gene:50484
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP563964.RA-B_MM97Nixngyj4Yo8NkmiS_Oc4H44S3MTlZQZUaGK4130_provenance
{
dgn-np:NP563964.RA-B_MM97Nixngyj4Yo8NkmiS_Oc4H44S3MTlZQZUaGK4130_assertion
dcterms:description
"[p53R2 is directly induced by wild-type p53 and involved in the p53 checkpoint for repair of damaged DNA, raising the possibility that mutational inactivation of p53R2 may contribute to the development and progression of human malignancies.]. 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:11920641
;
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:NP563964.RA-B_MM97Nixngyj4Yo8NkmiS_Oc4H44S3MTlZQZUaGK4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:40+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" .
}