@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP310580.RAtmY6SqGtXgQeHrTfPGH05xW77FS8jJ2gp_yO_vQVUn4
> .
@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:NP310580.RAtmY6SqGtXgQeHrTfPGH05xW77FS8jJ2gp_yO_vQVUn4130_head
{
this:
np:hasAssertion
dgn-np:NP310580.RAtmY6SqGtXgQeHrTfPGH05xW77FS8jJ2gp_yO_vQVUn4130_assertion
;
np:hasProvenance
dgn-np:NP310580.RAtmY6SqGtXgQeHrTfPGH05xW77FS8jJ2gp_yO_vQVUn4130_provenance
;
np:hasPublicationInfo
dgn-np:NP310580.RAtmY6SqGtXgQeHrTfPGH05xW77FS8jJ2gp_yO_vQVUn4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP310580.RAtmY6SqGtXgQeHrTfPGH05xW77FS8jJ2gp_yO_vQVUn4130_assertion
a
np:Assertion
.
dgn-np:NP310580.RAtmY6SqGtXgQeHrTfPGH05xW77FS8jJ2gp_yO_vQVUn4130_provenance
a
np:Provenance
.
dgn-np:NP310580.RAtmY6SqGtXgQeHrTfPGH05xW77FS8jJ2gp_yO_vQVUn4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP310580.RAtmY6SqGtXgQeHrTfPGH05xW77FS8jJ2gp_yO_vQVUn4130_assertion
{
miriam-gene:51639
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN2c648059ab9148d82437605e65350c77
sio:SIO_000628
miriam-gene:51639
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP310580.RAtmY6SqGtXgQeHrTfPGH05xW77FS8jJ2gp_yO_vQVUn4130_provenance
{
dgn-np:NP310580.RAtmY6SqGtXgQeHrTfPGH05xW77FS8jJ2gp_yO_vQVUn4130_assertion
dcterms:description
"[Thus, these data support a new model in which overcoming senescence plays a critical role in human cancer pathogenesis and requires at least two genetic changes that occur in several combinations that can include either p16 or pRb loss and at least one additional alteration, such as +20q11-q12, -3p13-p14, or -8p21-pter.]. 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:9436977
;
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:NP310580.RAtmY6SqGtXgQeHrTfPGH05xW77FS8jJ2gp_yO_vQVUn4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:58+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" .
}