@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP922308.RAxVFO1t_tHHpq0uyMuG2Skbza0xHPUHdSaAXtWF6Ptq8
> .
@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:NP922308.RAxVFO1t_tHHpq0uyMuG2Skbza0xHPUHdSaAXtWF6Ptq8130_head
{
this:
np:hasAssertion
dgn-np:NP922308.RAxVFO1t_tHHpq0uyMuG2Skbza0xHPUHdSaAXtWF6Ptq8130_assertion
;
np:hasProvenance
dgn-np:NP922308.RAxVFO1t_tHHpq0uyMuG2Skbza0xHPUHdSaAXtWF6Ptq8130_provenance
;
np:hasPublicationInfo
dgn-np:NP922308.RAxVFO1t_tHHpq0uyMuG2Skbza0xHPUHdSaAXtWF6Ptq8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP922308.RAxVFO1t_tHHpq0uyMuG2Skbza0xHPUHdSaAXtWF6Ptq8130_assertion
a
np:Assertion
.
dgn-np:NP922308.RAxVFO1t_tHHpq0uyMuG2Skbza0xHPUHdSaAXtWF6Ptq8130_provenance
a
np:Provenance
.
dgn-np:NP922308.RAxVFO1t_tHHpq0uyMuG2Skbza0xHPUHdSaAXtWF6Ptq8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP922308.RAxVFO1t_tHHpq0uyMuG2Skbza0xHPUHdSaAXtWF6Ptq8130_assertion
{
miriam-gene:1871
a
ncit:C16612
.
lld:C0178874
a
ncit:C7057
.
dgn-gda:DGN28a33fd7b650db62ce981b61c7331472
sio:SIO_000628
miriam-gene:1871
,
lld:C0178874
;
a
sio:SIO_001121
.
}
dgn-np:NP922308.RAxVFO1t_tHHpq0uyMuG2Skbza0xHPUHdSaAXtWF6Ptq8130_provenance
{
dgn-np:NP922308.RAxVFO1t_tHHpq0uyMuG2Skbza0xHPUHdSaAXtWF6Ptq8130_assertion
dcterms:description
"[Our results suggest that MDM4 gain may be involved in the early transition from normal retina to retinoma, while MYCN and E2F3 progressive gain may represent driving factors of tumor 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: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:NP922308.RAxVFO1t_tHHpq0uyMuG2Skbza0xHPUHdSaAXtWF6Ptq8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:26+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" .
}