@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP793177.RAP3dYoA84i81FtCNhzCAayXZpb9ME_6w02ZdDVpAV9fw
> .
@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:NP793177.RAP3dYoA84i81FtCNhzCAayXZpb9ME_6w02ZdDVpAV9fw130_head
{
this:
np:hasAssertion
dgn-np:NP793177.RAP3dYoA84i81FtCNhzCAayXZpb9ME_6w02ZdDVpAV9fw130_assertion
;
np:hasProvenance
dgn-np:NP793177.RAP3dYoA84i81FtCNhzCAayXZpb9ME_6w02ZdDVpAV9fw130_provenance
;
np:hasPublicationInfo
dgn-np:NP793177.RAP3dYoA84i81FtCNhzCAayXZpb9ME_6w02ZdDVpAV9fw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP793177.RAP3dYoA84i81FtCNhzCAayXZpb9ME_6w02ZdDVpAV9fw130_assertion
a
np:Assertion
.
dgn-np:NP793177.RAP3dYoA84i81FtCNhzCAayXZpb9ME_6w02ZdDVpAV9fw130_provenance
a
np:Provenance
.
dgn-np:NP793177.RAP3dYoA84i81FtCNhzCAayXZpb9ME_6w02ZdDVpAV9fw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP793177.RAP3dYoA84i81FtCNhzCAayXZpb9ME_6w02ZdDVpAV9fw130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0027149
a
ncit:C7057
.
dgn-gda:DGN78e254a82ac605af0279c588fec56757
sio:SIO_000628
miriam-gene:7157
,
lld:C0027149
;
a
sio:SIO_001121
.
}
dgn-np:NP793177.RAP3dYoA84i81FtCNhzCAayXZpb9ME_6w02ZdDVpAV9fw130_provenance
{
dgn-np:NP793177.RAP3dYoA84i81FtCNhzCAayXZpb9ME_6w02ZdDVpAV9fw130_assertion
dcterms:description
"[We report here that both reovirus and myxoma virus preferentially infect cancer cells bearing dysfunctional or deleted p53, ATM and Rb tumor suppressor genes compared to cells retaining normal counterparts of these genes.]. 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:20473328
;
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:NP793177.RAP3dYoA84i81FtCNhzCAayXZpb9ME_6w02ZdDVpAV9fw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:07+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" .
}