@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP807931.RA7iNQuQ5ZjLbjg_QEUKZd-hmyglQeYhW5U9GRLjjPvjc
> .
@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:NP807931.RA7iNQuQ5ZjLbjg_QEUKZd-hmyglQeYhW5U9GRLjjPvjc130_head
{
this:
np:hasAssertion
dgn-np:NP807931.RA7iNQuQ5ZjLbjg_QEUKZd-hmyglQeYhW5U9GRLjjPvjc130_assertion
;
np:hasProvenance
dgn-np:NP807931.RA7iNQuQ5ZjLbjg_QEUKZd-hmyglQeYhW5U9GRLjjPvjc130_provenance
;
np:hasPublicationInfo
dgn-np:NP807931.RA7iNQuQ5ZjLbjg_QEUKZd-hmyglQeYhW5U9GRLjjPvjc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP807931.RA7iNQuQ5ZjLbjg_QEUKZd-hmyglQeYhW5U9GRLjjPvjc130_assertion
a
np:Assertion
.
dgn-np:NP807931.RA7iNQuQ5ZjLbjg_QEUKZd-hmyglQeYhW5U9GRLjjPvjc130_provenance
a
np:Provenance
.
dgn-np:NP807931.RA7iNQuQ5ZjLbjg_QEUKZd-hmyglQeYhW5U9GRLjjPvjc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP807931.RA7iNQuQ5ZjLbjg_QEUKZd-hmyglQeYhW5U9GRLjjPvjc130_assertion
{
miriam-gene:9034
a
ncit:C16612
.
lld:C0085390
a
ncit:C7057
.
dgn-gda:DGN8e5c43fe0840484fbfa4951db67d5682
sio:SIO_000628
miriam-gene:9034
,
lld:C0085390
;
a
sio:SIO_001121
.
}
dgn-np:NP807931.RA7iNQuQ5ZjLbjg_QEUKZd-hmyglQeYhW5U9GRLjjPvjc130_provenance
{
dgn-np:NP807931.RA7iNQuQ5ZjLbjg_QEUKZd-hmyglQeYhW5U9GRLjjPvjc130_assertion
dcterms:description
"[In order to examine further the requirement for p53 in HSER and UVER, we have examined host cell reactivation (HCR) of the reporter construct in HS treated, UV treated and mock treated Li-Fraumeni syndrome (LFS) fibroblasts, which are heterozygous for a p53 mutation, and immortalized LFS cell sublines, which express only mutant 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:9054614
;
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:NP807931.RA7iNQuQ5ZjLbjg_QEUKZd-hmyglQeYhW5U9GRLjjPvjc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:15+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" .
}