@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP744896.RAw4CAmcgOyn5eOrzmNVpWVXnEg8B2v9jTwgCMD7WkZ84
> .
@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:NP744896.RAw4CAmcgOyn5eOrzmNVpWVXnEg8B2v9jTwgCMD7WkZ84130_head
{
this:
np:hasAssertion
dgn-np:NP744896.RAw4CAmcgOyn5eOrzmNVpWVXnEg8B2v9jTwgCMD7WkZ84130_assertion
;
np:hasProvenance
dgn-np:NP744896.RAw4CAmcgOyn5eOrzmNVpWVXnEg8B2v9jTwgCMD7WkZ84130_provenance
;
np:hasPublicationInfo
dgn-np:NP744896.RAw4CAmcgOyn5eOrzmNVpWVXnEg8B2v9jTwgCMD7WkZ84130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP744896.RAw4CAmcgOyn5eOrzmNVpWVXnEg8B2v9jTwgCMD7WkZ84130_assertion
a
np:Assertion
.
dgn-np:NP744896.RAw4CAmcgOyn5eOrzmNVpWVXnEg8B2v9jTwgCMD7WkZ84130_provenance
a
np:Provenance
.
dgn-np:NP744896.RAw4CAmcgOyn5eOrzmNVpWVXnEg8B2v9jTwgCMD7WkZ84130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP744896.RAw4CAmcgOyn5eOrzmNVpWVXnEg8B2v9jTwgCMD7WkZ84130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C1332922
a
ncit:C7057
.
dgn-gda:DGN7f97e85f632244fe8b0d774f7303cc5b
sio:SIO_000628
miriam-gene:7157
,
lld:C1332922
;
a
sio:SIO_001121
.
}
dgn-np:NP744896.RAw4CAmcgOyn5eOrzmNVpWVXnEg8B2v9jTwgCMD7WkZ84130_provenance
{
dgn-np:NP744896.RAw4CAmcgOyn5eOrzmNVpWVXnEg8B2v9jTwgCMD7WkZ84130_assertion
dcterms:description
"[These results suggest that inactivation of p53 may allow lung cancer cells to go through an inappropriate second division cycle under certain forms of mitotic stresses, which would result in the induction of the CIN phenotype in conjunction with the generation of aneuploidy.]. 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:11583962
;
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:NP744896.RAw4CAmcgOyn5eOrzmNVpWVXnEg8B2v9jTwgCMD7WkZ84130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:31+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" .
}