@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP250588.RABJx3SWbtqPbhFcPLdky4XlnC8yL2K_8sLq5XawisUUA
> .
@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:NP250588.RABJx3SWbtqPbhFcPLdky4XlnC8yL2K_8sLq5XawisUUA130_head
{
this:
np:hasAssertion
dgn-np:NP250588.RABJx3SWbtqPbhFcPLdky4XlnC8yL2K_8sLq5XawisUUA130_assertion
;
np:hasProvenance
dgn-np:NP250588.RABJx3SWbtqPbhFcPLdky4XlnC8yL2K_8sLq5XawisUUA130_provenance
;
np:hasPublicationInfo
dgn-np:NP250588.RABJx3SWbtqPbhFcPLdky4XlnC8yL2K_8sLq5XawisUUA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP250588.RABJx3SWbtqPbhFcPLdky4XlnC8yL2K_8sLq5XawisUUA130_assertion
a
np:Assertion
.
dgn-np:NP250588.RABJx3SWbtqPbhFcPLdky4XlnC8yL2K_8sLq5XawisUUA130_provenance
a
np:Provenance
.
dgn-np:NP250588.RABJx3SWbtqPbhFcPLdky4XlnC8yL2K_8sLq5XawisUUA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP250588.RABJx3SWbtqPbhFcPLdky4XlnC8yL2K_8sLq5XawisUUA130_assertion
{
miriam-gene:23291
a
ncit:C16612
.
lld:C0585442
a
ncit:C7057
.
dgn-gda:DGNce9a320ac38e2222fac23bc2461e5cde
sio:SIO_000628
miriam-gene:23291
,
lld:C0585442
;
a
sio:SIO_001121
.
}
dgn-np:NP250588.RABJx3SWbtqPbhFcPLdky4XlnC8yL2K_8sLq5XawisUUA130_provenance
{
dgn-np:NP250588.RABJx3SWbtqPbhFcPLdky4XlnC8yL2K_8sLq5XawisUUA130_assertion
dcterms:description
"[We also investigated whether there was an association between TP53 mutation and centrosome aberrations in the generation of chromosomal aneuploidy in OS in four OS cell lines (HOS, SAOS2, U2OS, and MG63) and in a subset of seven tumors.]. 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:12850370
;
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:NP250588.RABJx3SWbtqPbhFcPLdky4XlnC8yL2K_8sLq5XawisUUA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:20+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" .
}