@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP421454.RAcAXNQKnU7tSWfzC7U32hnLlp8LG1BhymfCiJ6zFoUmE
> .
@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:NP421454.RAcAXNQKnU7tSWfzC7U32hnLlp8LG1BhymfCiJ6zFoUmE130_head
{
this:
np:hasAssertion
dgn-np:NP421454.RAcAXNQKnU7tSWfzC7U32hnLlp8LG1BhymfCiJ6zFoUmE130_assertion
;
np:hasProvenance
dgn-np:NP421454.RAcAXNQKnU7tSWfzC7U32hnLlp8LG1BhymfCiJ6zFoUmE130_provenance
;
np:hasPublicationInfo
dgn-np:NP421454.RAcAXNQKnU7tSWfzC7U32hnLlp8LG1BhymfCiJ6zFoUmE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP421454.RAcAXNQKnU7tSWfzC7U32hnLlp8LG1BhymfCiJ6zFoUmE130_assertion
a
np:Assertion
.
dgn-np:NP421454.RAcAXNQKnU7tSWfzC7U32hnLlp8LG1BhymfCiJ6zFoUmE130_provenance
a
np:Provenance
.
dgn-np:NP421454.RAcAXNQKnU7tSWfzC7U32hnLlp8LG1BhymfCiJ6zFoUmE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP421454.RAcAXNQKnU7tSWfzC7U32hnLlp8LG1BhymfCiJ6zFoUmE130_assertion
{
miriam-gene:4194
a
ncit:C16612
.
lld:C1266186
a
ncit:C7057
.
dgn-gda:DGNff3dbcefc6ba262904e92d7a0e3ed152
sio:SIO_000628
miriam-gene:4194
,
lld:C1266186
;
a
sio:SIO_001121
.
}
dgn-np:NP421454.RAcAXNQKnU7tSWfzC7U32hnLlp8LG1BhymfCiJ6zFoUmE130_provenance
{
dgn-np:NP421454.RAcAXNQKnU7tSWfzC7U32hnLlp8LG1BhymfCiJ6zFoUmE130_assertion
dcterms:description
"[Our results demonstrated that some copy number changes thought to belong to early (MDM4 gain) or late stage (MYCN and E2F3 gain) of retinoblastoma are already present in retinoma at the same (for MDM4) or at lower (for MYCN and E2F3) copy number variation respect to retinoblastoma.]. 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:18785023
;
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:NP421454.RAcAXNQKnU7tSWfzC7U32hnLlp8LG1BhymfCiJ6zFoUmE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:10+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" .
}