@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP679235.RAFQ63tX6p8Canoy0pBauMCBLTCjpfRA9_n9LWx3N43I4
> .
@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:NP679235.RAFQ63tX6p8Canoy0pBauMCBLTCjpfRA9_n9LWx3N43I4130_head
{
this:
np:hasAssertion
dgn-np:NP679235.RAFQ63tX6p8Canoy0pBauMCBLTCjpfRA9_n9LWx3N43I4130_assertion
;
np:hasProvenance
dgn-np:NP679235.RAFQ63tX6p8Canoy0pBauMCBLTCjpfRA9_n9LWx3N43I4130_provenance
;
np:hasPublicationInfo
dgn-np:NP679235.RAFQ63tX6p8Canoy0pBauMCBLTCjpfRA9_n9LWx3N43I4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP679235.RAFQ63tX6p8Canoy0pBauMCBLTCjpfRA9_n9LWx3N43I4130_assertion
a
np:Assertion
.
dgn-np:NP679235.RAFQ63tX6p8Canoy0pBauMCBLTCjpfRA9_n9LWx3N43I4130_provenance
a
np:Provenance
.
dgn-np:NP679235.RAFQ63tX6p8Canoy0pBauMCBLTCjpfRA9_n9LWx3N43I4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP679235.RAFQ63tX6p8Canoy0pBauMCBLTCjpfRA9_n9LWx3N43I4130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C1704429
a
ncit:C7057
.
dgn-gda:DGN427b508a439cefac3bb22878fe53fdf3
sio:SIO_000628
miriam-gene:7157
,
lld:C1704429
;
a
sio:SIO_001121
.
}
dgn-np:NP679235.RAFQ63tX6p8Canoy0pBauMCBLTCjpfRA9_n9LWx3N43I4130_provenance
{
dgn-np:NP679235.RAFQ63tX6p8Canoy0pBauMCBLTCjpfRA9_n9LWx3N43I4130_assertion
dcterms:description
"[Here we report that in human cells, Chk2 and p53 form protein-protein complexes whose abundance increased upon DNA damage, and whose formation was abrogated through cancer associated mutations in the FHA domain of Chk2, or mutations in the tetramerization domain of p53.]. 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:11571648
;
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:NP679235.RAFQ63tX6p8Canoy0pBauMCBLTCjpfRA9_n9LWx3N43I4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:50+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" .
}