@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP339593.RACGB_IUEZU8KOS1zmL2MG3RLwRWHic-ybYKEsi9ss3nU
> .
@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:NP339593.RACGB_IUEZU8KOS1zmL2MG3RLwRWHic-ybYKEsi9ss3nU130_head
{
this:
np:hasAssertion
dgn-np:NP339593.RACGB_IUEZU8KOS1zmL2MG3RLwRWHic-ybYKEsi9ss3nU130_assertion
;
np:hasProvenance
dgn-np:NP339593.RACGB_IUEZU8KOS1zmL2MG3RLwRWHic-ybYKEsi9ss3nU130_provenance
;
np:hasPublicationInfo
dgn-np:NP339593.RACGB_IUEZU8KOS1zmL2MG3RLwRWHic-ybYKEsi9ss3nU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP339593.RACGB_IUEZU8KOS1zmL2MG3RLwRWHic-ybYKEsi9ss3nU130_assertion
a
np:Assertion
.
dgn-np:NP339593.RACGB_IUEZU8KOS1zmL2MG3RLwRWHic-ybYKEsi9ss3nU130_provenance
a
np:Provenance
.
dgn-np:NP339593.RACGB_IUEZU8KOS1zmL2MG3RLwRWHic-ybYKEsi9ss3nU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP339593.RACGB_IUEZU8KOS1zmL2MG3RLwRWHic-ybYKEsi9ss3nU130_assertion
{
miriam-gene:7015
a
ncit:C16612
.
lld:C0029925
a
ncit:C7057
.
dgn-gda:DGN721db094393517ddd2f1880d8eda049b
sio:SIO_000628
miriam-gene:7015
,
lld:C0029925
;
a
sio:SIO_001121
.
}
dgn-np:NP339593.RACGB_IUEZU8KOS1zmL2MG3RLwRWHic-ybYKEsi9ss3nU130_provenance
{
dgn-np:NP339593.RACGB_IUEZU8KOS1zmL2MG3RLwRWHic-ybYKEsi9ss3nU130_assertion
dcterms:description
"[As both Rb and hTERT pathways are commonly altered in human ovarian cancer and these genetic changes are faithfully modeled in these cells without using viral protein, these immortal cells represent an authentic in vitro model system with which to study the initiation and progression of human ovarian cancer.]. 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:16953228
;
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:NP339593.RACGB_IUEZU8KOS1zmL2MG3RLwRWHic-ybYKEsi9ss3nU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:19+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" .
}