@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP718348.RA5stq3jgSNiyf8IjWrpwx-KC-GzpqTaLpucA8lgaILr4
> .
@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:NP718348.RA5stq3jgSNiyf8IjWrpwx-KC-GzpqTaLpucA8lgaILr4130_head
{
this:
np:hasAssertion
dgn-np:NP718348.RA5stq3jgSNiyf8IjWrpwx-KC-GzpqTaLpucA8lgaILr4130_assertion
;
np:hasProvenance
dgn-np:NP718348.RA5stq3jgSNiyf8IjWrpwx-KC-GzpqTaLpucA8lgaILr4130_provenance
;
np:hasPublicationInfo
dgn-np:NP718348.RA5stq3jgSNiyf8IjWrpwx-KC-GzpqTaLpucA8lgaILr4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP718348.RA5stq3jgSNiyf8IjWrpwx-KC-GzpqTaLpucA8lgaILr4130_assertion
a
np:Assertion
.
dgn-np:NP718348.RA5stq3jgSNiyf8IjWrpwx-KC-GzpqTaLpucA8lgaILr4130_provenance
a
np:Provenance
.
dgn-np:NP718348.RA5stq3jgSNiyf8IjWrpwx-KC-GzpqTaLpucA8lgaILr4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP718348.RA5stq3jgSNiyf8IjWrpwx-KC-GzpqTaLpucA8lgaILr4130_assertion
{
miriam-gene:5001
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGNdab0004162076c060c75d3f9a026bab9
sio:SIO_000628
miriam-gene:5001
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP718348.RA5stq3jgSNiyf8IjWrpwx-KC-GzpqTaLpucA8lgaILr4130_provenance
{
dgn-np:NP718348.RA5stq3jgSNiyf8IjWrpwx-KC-GzpqTaLpucA8lgaILr4130_assertion
dcterms:description
"[Because of its localization within a region that is commonly deleted in patients with myeloid malignancies and because of the implication of its protein product in cell cycle control (DNA replication) and regulation of gene expression (transcriptional silencing), ORC5L appeared to be a candidate tumor suppressor gene for myeloid disorders associated with 7q22 deletions.]. 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:11379876
;
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:NP718348.RA5stq3jgSNiyf8IjWrpwx-KC-GzpqTaLpucA8lgaILr4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:16+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" .
}