@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP791235.RA2SJ7x1a1v93F5yscUWaWleLqcDz6ftLKqCXryH2msFU
> .
@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:NP791235.RA2SJ7x1a1v93F5yscUWaWleLqcDz6ftLKqCXryH2msFU130_head
{
this:
np:hasAssertion
dgn-np:NP791235.RA2SJ7x1a1v93F5yscUWaWleLqcDz6ftLKqCXryH2msFU130_assertion
;
np:hasProvenance
dgn-np:NP791235.RA2SJ7x1a1v93F5yscUWaWleLqcDz6ftLKqCXryH2msFU130_provenance
;
np:hasPublicationInfo
dgn-np:NP791235.RA2SJ7x1a1v93F5yscUWaWleLqcDz6ftLKqCXryH2msFU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP791235.RA2SJ7x1a1v93F5yscUWaWleLqcDz6ftLKqCXryH2msFU130_assertion
a
np:Assertion
.
dgn-np:NP791235.RA2SJ7x1a1v93F5yscUWaWleLqcDz6ftLKqCXryH2msFU130_provenance
a
np:Provenance
.
dgn-np:NP791235.RA2SJ7x1a1v93F5yscUWaWleLqcDz6ftLKqCXryH2msFU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP791235.RA2SJ7x1a1v93F5yscUWaWleLqcDz6ftLKqCXryH2msFU130_assertion
{
miriam-gene:8021
a
ncit:C16612
.
lld:C0023473
a
ncit:C7057
.
dgn-gda:DGNbacbc20b0eb6a197aca171e005cb359d
sio:SIO_000628
miriam-gene:8021
,
lld:C0023473
;
a
sio:SIO_001121
.
}
dgn-np:NP791235.RA2SJ7x1a1v93F5yscUWaWleLqcDz6ftLKqCXryH2msFU130_provenance
{
dgn-np:NP791235.RA2SJ7x1a1v93F5yscUWaWleLqcDz6ftLKqCXryH2msFU130_assertion
dcterms:description
"[Point mutations in p53 have been found in some cases of blast crisis and CML blastic cell lines, but it is not clear whether complete inactivation of p53 tumor suppressor function, with or without the production of a mutant protein, can by itself trigger the process of blastic transformation.]. 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:8282066
;
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:NP791235.RA2SJ7x1a1v93F5yscUWaWleLqcDz6ftLKqCXryH2msFU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:05+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" .
}