@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP200798.RA5XcmkvSwUs28yl4ZZylALFj5nVvkbTruNO_lUJ9tuS4
> .
@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:NP200798.RA5XcmkvSwUs28yl4ZZylALFj5nVvkbTruNO_lUJ9tuS4130_head
{
this:
np:hasAssertion
dgn-np:NP200798.RA5XcmkvSwUs28yl4ZZylALFj5nVvkbTruNO_lUJ9tuS4130_assertion
;
np:hasProvenance
dgn-np:NP200798.RA5XcmkvSwUs28yl4ZZylALFj5nVvkbTruNO_lUJ9tuS4130_provenance
;
np:hasPublicationInfo
dgn-np:NP200798.RA5XcmkvSwUs28yl4ZZylALFj5nVvkbTruNO_lUJ9tuS4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP200798.RA5XcmkvSwUs28yl4ZZylALFj5nVvkbTruNO_lUJ9tuS4130_assertion
a
np:Assertion
.
dgn-np:NP200798.RA5XcmkvSwUs28yl4ZZylALFj5nVvkbTruNO_lUJ9tuS4130_provenance
a
np:Provenance
.
dgn-np:NP200798.RA5XcmkvSwUs28yl4ZZylALFj5nVvkbTruNO_lUJ9tuS4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP200798.RA5XcmkvSwUs28yl4ZZylALFj5nVvkbTruNO_lUJ9tuS4130_assertion
{
miriam-gene:2321
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN9e59ee95f66f9458111cc3e81bb9a70b
sio:SIO_000628
miriam-gene:2321
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP200798.RA5XcmkvSwUs28yl4ZZylALFj5nVvkbTruNO_lUJ9tuS4130_provenance
{
dgn-np:NP200798.RA5XcmkvSwUs28yl4ZZylALFj5nVvkbTruNO_lUJ9tuS4130_assertion
dcterms:description
"[p53(FRT) mice will enable dual recombinase technology to study cancer biology because Cre is available to modify genes specifically in stromal cells to investigate their role in tumor development, progression and response to therapy.]. 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:22228755
;
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:NP200798.RA5XcmkvSwUs28yl4ZZylALFj5nVvkbTruNO_lUJ9tuS4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:50+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" .
}