@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP816573.RAmk0tpPtDr-YpVvSwSiUeilYl4XAIYeZLpVCCmekdBR4
> .
@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:NP816573.RAmk0tpPtDr-YpVvSwSiUeilYl4XAIYeZLpVCCmekdBR4130_head
{
this:
np:hasAssertion
dgn-np:NP816573.RAmk0tpPtDr-YpVvSwSiUeilYl4XAIYeZLpVCCmekdBR4130_assertion
;
np:hasProvenance
dgn-np:NP816573.RAmk0tpPtDr-YpVvSwSiUeilYl4XAIYeZLpVCCmekdBR4130_provenance
;
np:hasPublicationInfo
dgn-np:NP816573.RAmk0tpPtDr-YpVvSwSiUeilYl4XAIYeZLpVCCmekdBR4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP816573.RAmk0tpPtDr-YpVvSwSiUeilYl4XAIYeZLpVCCmekdBR4130_assertion
a
np:Assertion
.
dgn-np:NP816573.RAmk0tpPtDr-YpVvSwSiUeilYl4XAIYeZLpVCCmekdBR4130_provenance
a
np:Provenance
.
dgn-np:NP816573.RAmk0tpPtDr-YpVvSwSiUeilYl4XAIYeZLpVCCmekdBR4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP816573.RAmk0tpPtDr-YpVvSwSiUeilYl4XAIYeZLpVCCmekdBR4130_assertion
{
miriam-gene:6121
a
ncit:C16612
.
lld:C0027627
a
ncit:C7057
.
dgn-gda:DGNa898d8bc85fe167ddcd863fae7d4c168
sio:SIO_000628
miriam-gene:6121
,
lld:C0027627
;
a
sio:SIO_001121
.
}
dgn-np:NP816573.RAmk0tpPtDr-YpVvSwSiUeilYl4XAIYeZLpVCCmekdBR4130_provenance
{
dgn-np:NP816573.RAmk0tpPtDr-YpVvSwSiUeilYl4XAIYeZLpVCCmekdBR4130_assertion
dcterms:description
"[Moreover, recent data suggests that expression of mutant p53 is not the equivalent of p53 loss, and that mutant p53s can acquire new functions to drive cell migration, invasion, and metastasis, in part by interfering with p63 function.]. 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:21263025
;
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:NP816573.RAmk0tpPtDr-YpVvSwSiUeilYl4XAIYeZLpVCCmekdBR4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:20+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" .
}