@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP586129.RAvVDF23LrKxyKGm-k1Fhwg35Q5L0WE3h-hnvKYen7Czc
> .
@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:NP586129.RAvVDF23LrKxyKGm-k1Fhwg35Q5L0WE3h-hnvKYen7Czc130_head
{
this:
np:hasAssertion
dgn-np:NP586129.RAvVDF23LrKxyKGm-k1Fhwg35Q5L0WE3h-hnvKYen7Czc130_assertion
;
np:hasProvenance
dgn-np:NP586129.RAvVDF23LrKxyKGm-k1Fhwg35Q5L0WE3h-hnvKYen7Czc130_provenance
;
np:hasPublicationInfo
dgn-np:NP586129.RAvVDF23LrKxyKGm-k1Fhwg35Q5L0WE3h-hnvKYen7Czc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP586129.RAvVDF23LrKxyKGm-k1Fhwg35Q5L0WE3h-hnvKYen7Czc130_assertion
a
np:Assertion
.
dgn-np:NP586129.RAvVDF23LrKxyKGm-k1Fhwg35Q5L0WE3h-hnvKYen7Czc130_provenance
a
np:Provenance
.
dgn-np:NP586129.RAvVDF23LrKxyKGm-k1Fhwg35Q5L0WE3h-hnvKYen7Czc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP586129.RAvVDF23LrKxyKGm-k1Fhwg35Q5L0WE3h-hnvKYen7Czc130_assertion
{
miriam-gene:1406
a
ncit:C16612
.
lld:C0035335
a
ncit:C7057
.
dgn-gda:DGNd7c1db8dd7d3022563eef1c5f4720ae4
sio:SIO_000628
miriam-gene:1406
,
lld:C0035335
;
a
sio:SIO_001121
.
}
dgn-np:NP586129.RAvVDF23LrKxyKGm-k1Fhwg35Q5L0WE3h-hnvKYen7Czc130_provenance
{
dgn-np:NP586129.RAvVDF23LrKxyKGm-k1Fhwg35Q5L0WE3h-hnvKYen7Czc130_assertion
dcterms:description
"[Both CRX and OTX2 are widely expressed in retinoblastoma cell lines and in retinoblastoma tumors, although CRX is more abundant than OTX2 in the differentiated elements of retinoblastoma tumors such as large rosettes, Flexner-Wintersteiner rosettes and fleurettes.]. 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:19686387
;
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:NP586129.RAvVDF23LrKxyKGm-k1Fhwg35Q5L0WE3h-hnvKYen7Czc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:53+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" .
}