@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP275442.RAiLyqKzcbUuLQ8Hgv8qMuitSIv80wvu4BXBRgvAiksZ0
> .
@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:NP275442.RAiLyqKzcbUuLQ8Hgv8qMuitSIv80wvu4BXBRgvAiksZ0130_head
{
this:
np:hasAssertion
dgn-np:NP275442.RAiLyqKzcbUuLQ8Hgv8qMuitSIv80wvu4BXBRgvAiksZ0130_assertion
;
np:hasProvenance
dgn-np:NP275442.RAiLyqKzcbUuLQ8Hgv8qMuitSIv80wvu4BXBRgvAiksZ0130_provenance
;
np:hasPublicationInfo
dgn-np:NP275442.RAiLyqKzcbUuLQ8Hgv8qMuitSIv80wvu4BXBRgvAiksZ0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP275442.RAiLyqKzcbUuLQ8Hgv8qMuitSIv80wvu4BXBRgvAiksZ0130_assertion
a
np:Assertion
.
dgn-np:NP275442.RAiLyqKzcbUuLQ8Hgv8qMuitSIv80wvu4BXBRgvAiksZ0130_provenance
a
np:Provenance
.
dgn-np:NP275442.RAiLyqKzcbUuLQ8Hgv8qMuitSIv80wvu4BXBRgvAiksZ0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP275442.RAiLyqKzcbUuLQ8Hgv8qMuitSIv80wvu4BXBRgvAiksZ0130_assertion
{
miriam-gene:1111
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN94ee6b1aaa773e91337b604cb8c18177
sio:SIO_000628
miriam-gene:1111
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP275442.RAiLyqKzcbUuLQ8Hgv8qMuitSIv80wvu4BXBRgvAiksZ0130_provenance
{
dgn-np:NP275442.RAiLyqKzcbUuLQ8Hgv8qMuitSIv80wvu4BXBRgvAiksZ0130_assertion
dcterms:description
"[Defects in p53 function, which occur frequently in human cancers due to mutations in TP53 or disruptions in the p53 regulatory pathway, render cells dependent on CHK1 (Checkpoint Kinase 1) to activate cell cycle checkpoints.]. 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:21087899
;
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:NP275442.RAiLyqKzcbUuLQ8Hgv8qMuitSIv80wvu4BXBRgvAiksZ0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:35+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" .
}