@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1071875.RA8F0tLBYMDI4TrRLlyNFInwbQ0PL2SUUnaHg2PtCCJAg
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1071875.RA8F0tLBYMDI4TrRLlyNFInwbQ0PL2SUUnaHg2PtCCJAg130_head
{
this:
np:hasAssertion
dgn-np:NP1071875.RA8F0tLBYMDI4TrRLlyNFInwbQ0PL2SUUnaHg2PtCCJAg130_assertion
;
np:hasProvenance
dgn-np:NP1071875.RA8F0tLBYMDI4TrRLlyNFInwbQ0PL2SUUnaHg2PtCCJAg130_provenance
;
np:hasPublicationInfo
dgn-np:NP1071875.RA8F0tLBYMDI4TrRLlyNFInwbQ0PL2SUUnaHg2PtCCJAg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1071875.RA8F0tLBYMDI4TrRLlyNFInwbQ0PL2SUUnaHg2PtCCJAg130_assertion
a
np:Assertion
.
dgn-np:NP1071875.RA8F0tLBYMDI4TrRLlyNFInwbQ0PL2SUUnaHg2PtCCJAg130_provenance
a
np:Provenance
.
dgn-np:NP1071875.RA8F0tLBYMDI4TrRLlyNFInwbQ0PL2SUUnaHg2PtCCJAg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1071875.RA8F0tLBYMDI4TrRLlyNFInwbQ0PL2SUUnaHg2PtCCJAg130_assertion
{
miriam-gene:129563
a
ncit:C16612
.
lld:C0796113
a
ncit:C7057
.
dgn-gda:DGNc6dd6b962964723a261d1b354c594320
sio:SIO_000628
miriam-gene:129563
,
lld:C0796113
;
a
sio:SIO_001121
.
}
dgn-np:NP1071875.RA8F0tLBYMDI4TrRLlyNFInwbQ0PL2SUUnaHg2PtCCJAg130_provenance
{
dgn-np:NP1071875.RA8F0tLBYMDI4TrRLlyNFInwbQ0PL2SUUnaHg2PtCCJAg130_assertion
dcterms:description
"[It has been postulated that the clinical features of Perlman syndrome result from disordered RNA metabolism and, though the precise targets of DIS3L2 have yet to be characterized, in cellular models DIS3L2 knockdown is associated with abnormalities of cell growth and division.]. 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:23613427
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1071875.RA8F0tLBYMDI4TrRLlyNFInwbQ0PL2SUUnaHg2PtCCJAg130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:52+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}