@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP798302.RAFaa3X5CDlG2-Olu2mkpQvMJ_qwNf-U6OJV9LvbE3yj8
> .
@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:NP798302.RAFaa3X5CDlG2-Olu2mkpQvMJ_qwNf-U6OJV9LvbE3yj8130_head
{
this:
np:hasAssertion
dgn-np:NP798302.RAFaa3X5CDlG2-Olu2mkpQvMJ_qwNf-U6OJV9LvbE3yj8130_assertion
;
np:hasProvenance
dgn-np:NP798302.RAFaa3X5CDlG2-Olu2mkpQvMJ_qwNf-U6OJV9LvbE3yj8130_provenance
;
np:hasPublicationInfo
dgn-np:NP798302.RAFaa3X5CDlG2-Olu2mkpQvMJ_qwNf-U6OJV9LvbE3yj8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP798302.RAFaa3X5CDlG2-Olu2mkpQvMJ_qwNf-U6OJV9LvbE3yj8130_assertion
a
np:Assertion
.
dgn-np:NP798302.RAFaa3X5CDlG2-Olu2mkpQvMJ_qwNf-U6OJV9LvbE3yj8130_provenance
a
np:Provenance
.
dgn-np:NP798302.RAFaa3X5CDlG2-Olu2mkpQvMJ_qwNf-U6OJV9LvbE3yj8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP798302.RAFaa3X5CDlG2-Olu2mkpQvMJ_qwNf-U6OJV9LvbE3yj8130_assertion
{
miriam-gene:3342
a
ncit:C16612
.
lld:C0085390
a
ncit:C7057
.
dgn-gda:DGNbe8923aad710086da97e405040531d8e
sio:SIO_000628
miriam-gene:3342
,
lld:C0085390
;
a
sio:SIO_001121
.
}
dgn-np:NP798302.RAFaa3X5CDlG2-Olu2mkpQvMJ_qwNf-U6OJV9LvbE3yj8130_provenance
{
dgn-np:NP798302.RAFaa3X5CDlG2-Olu2mkpQvMJ_qwNf-U6OJV9LvbE3yj8130_assertion
dcterms:description
"[Studies of Li-Fraumeni syndrome fibroblasts heterozygous for germline TP53 mutations have shown that loss of heterozygosity (LOH) occurs during passaging and is associated with genomic instability, such as chromosomal aberrations and aneuploidy to investigate the genomic changes associated with LOH in Li-Fraumeni (LF) fibroblasts, we have analysed cell strains at increasing population doublings (PD) using Comparative Genomic Hybridization (CGH).]. 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:10945493
;
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:NP798302.RAFaa3X5CDlG2-Olu2mkpQvMJ_qwNf-U6OJV9LvbE3yj8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:10+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" .
}