@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP261480.RAVQvCNj5LE76sxaafhQMyd9oCbUGt0qtM1UTbVM4rfXQ
> .
@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:NP261480.RAVQvCNj5LE76sxaafhQMyd9oCbUGt0qtM1UTbVM4rfXQ130_head
{
this:
np:hasAssertion
dgn-np:NP261480.RAVQvCNj5LE76sxaafhQMyd9oCbUGt0qtM1UTbVM4rfXQ130_assertion
;
np:hasProvenance
dgn-np:NP261480.RAVQvCNj5LE76sxaafhQMyd9oCbUGt0qtM1UTbVM4rfXQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP261480.RAVQvCNj5LE76sxaafhQMyd9oCbUGt0qtM1UTbVM4rfXQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP261480.RAVQvCNj5LE76sxaafhQMyd9oCbUGt0qtM1UTbVM4rfXQ130_assertion
a
np:Assertion
.
dgn-np:NP261480.RAVQvCNj5LE76sxaafhQMyd9oCbUGt0qtM1UTbVM4rfXQ130_provenance
a
np:Provenance
.
dgn-np:NP261480.RAVQvCNj5LE76sxaafhQMyd9oCbUGt0qtM1UTbVM4rfXQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP261480.RAVQvCNj5LE76sxaafhQMyd9oCbUGt0qtM1UTbVM4rfXQ130_assertion
{
miriam-gene:5111
a
ncit:C16612
.
lld:C2939419
a
ncit:C7057
.
dgn-gda:DGN81eedf980a32700e3c38e182f6a7886d
sio:SIO_000628
miriam-gene:5111
,
lld:C2939419
;
a
sio:SIO_001121
.
}
dgn-np:NP261480.RAVQvCNj5LE76sxaafhQMyd9oCbUGt0qtM1UTbVM4rfXQ130_provenance
{
dgn-np:NP261480.RAVQvCNj5LE76sxaafhQMyd9oCbUGt0qtM1UTbVM4rfXQ130_assertion
dcterms:description
"[Thus, recapitulation of aberrant cyclin E expression as seen in human premalignant and malignant lung lesions reproduces in the mouse frequent features of lung carcinogenesis, including CIN, Shh pathway activation, dysplasia, single or multiple lung cancers, or presence of metastases.]. 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:17360482
;
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:NP261480.RAVQvCNj5LE76sxaafhQMyd9oCbUGt0qtM1UTbVM4rfXQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:26+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" .
}