@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1258060.RA2vMu-riCl48PFCG_kh4Lw5obmkLk5G27ZdwVaTQXlPA
> .
@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:NP1258060.RA2vMu-riCl48PFCG_kh4Lw5obmkLk5G27ZdwVaTQXlPA130_head
{
this:
np:hasAssertion
dgn-np:NP1258060.RA2vMu-riCl48PFCG_kh4Lw5obmkLk5G27ZdwVaTQXlPA130_assertion
;
np:hasProvenance
dgn-np:NP1258060.RA2vMu-riCl48PFCG_kh4Lw5obmkLk5G27ZdwVaTQXlPA130_provenance
;
np:hasPublicationInfo
dgn-np:NP1258060.RA2vMu-riCl48PFCG_kh4Lw5obmkLk5G27ZdwVaTQXlPA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1258060.RA2vMu-riCl48PFCG_kh4Lw5obmkLk5G27ZdwVaTQXlPA130_assertion
a
np:Assertion
.
dgn-np:NP1258060.RA2vMu-riCl48PFCG_kh4Lw5obmkLk5G27ZdwVaTQXlPA130_provenance
a
np:Provenance
.
dgn-np:NP1258060.RA2vMu-riCl48PFCG_kh4Lw5obmkLk5G27ZdwVaTQXlPA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1258060.RA2vMu-riCl48PFCG_kh4Lw5obmkLk5G27ZdwVaTQXlPA130_assertion
{
miriam-gene:100288695
a
ncit:C16612
.
lld:C0041107
a
ncit:C7057
.
dgn-gda:DGN2e19d8d8313f48a59d5f16c230a03af4
sio:SIO_000628
miriam-gene:100288695
,
lld:C0041107
;
a
sio:SIO_001121
.
}
dgn-np:NP1258060.RA2vMu-riCl48PFCG_kh4Lw5obmkLk5G27ZdwVaTQXlPA130_provenance
{
dgn-np:NP1258060.RA2vMu-riCl48PFCG_kh4Lw5obmkLk5G27ZdwVaTQXlPA130_assertion
dcterms:description
"[The present study suggested that deletion of evolutionarily conserved developmental genes (RGPD5, RGPD and LIMS3) in the 2q13 region might have contributed to more severity in phenotype as compared to so far such reported cases of 18p trisomy's, as these are involved in nuclear-cytoplasm trafficking, signaling for tissue patterning and differentiation.]. 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:25617521
;
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:NP1258060.RA2vMu-riCl48PFCG_kh4Lw5obmkLk5G27ZdwVaTQXlPA130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:16+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: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" .
}