@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP727396.RADh1R5l37gG9pwvsrAcPZ66UBkSBMIJFNpjlvEiTMNvk
> .
@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:NP727396.RADh1R5l37gG9pwvsrAcPZ66UBkSBMIJFNpjlvEiTMNvk130_head
{
this:
np:hasAssertion
dgn-np:NP727396.RADh1R5l37gG9pwvsrAcPZ66UBkSBMIJFNpjlvEiTMNvk130_assertion
;
np:hasProvenance
dgn-np:NP727396.RADh1R5l37gG9pwvsrAcPZ66UBkSBMIJFNpjlvEiTMNvk130_provenance
;
np:hasPublicationInfo
dgn-np:NP727396.RADh1R5l37gG9pwvsrAcPZ66UBkSBMIJFNpjlvEiTMNvk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP727396.RADh1R5l37gG9pwvsrAcPZ66UBkSBMIJFNpjlvEiTMNvk130_assertion
a
np:Assertion
.
dgn-np:NP727396.RADh1R5l37gG9pwvsrAcPZ66UBkSBMIJFNpjlvEiTMNvk130_provenance
a
np:Provenance
.
dgn-np:NP727396.RADh1R5l37gG9pwvsrAcPZ66UBkSBMIJFNpjlvEiTMNvk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP727396.RADh1R5l37gG9pwvsrAcPZ66UBkSBMIJFNpjlvEiTMNvk130_assertion
{
miriam-gene:595
a
ncit:C16612
.
lld:C1947901
a
ncit:C7057
.
dgn-gda:DGN6f49d971fd9ecfcb9af62ad54a0bff59
sio:SIO_000628
miriam-gene:595
,
lld:C1947901
;
a
sio:SIO_001121
.
}
dgn-np:NP727396.RADh1R5l37gG9pwvsrAcPZ66UBkSBMIJFNpjlvEiTMNvk130_provenance
{
dgn-np:NP727396.RADh1R5l37gG9pwvsrAcPZ66UBkSBMIJFNpjlvEiTMNvk130_assertion
dcterms:description
"[It is of interest to evaluate concurrently the alterations of both genes on the same series of NSCLCs, to investigate whether cyclin D1 and RB alterations are alternative pathways leading to inactivation of the G1 restriction point or if they can occur in the same tumor, possibly exerting an additive effect on cancer progression.]. 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:9462706
;
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:NP727396.RADh1R5l37gG9pwvsrAcPZ66UBkSBMIJFNpjlvEiTMNvk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:21+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" .
}