@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP470727.RAgPCbJfwRtxHuiwd2sVu-0vqaZUoqOWn2IcSTu196mX8
> .
@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/v3.0.0/void/
> .
dgn-np:NP470727.RAgPCbJfwRtxHuiwd2sVu-0vqaZUoqOWn2IcSTu196mX8130_head
{
this:
np:hasAssertion
dgn-np:NP470727.RAgPCbJfwRtxHuiwd2sVu-0vqaZUoqOWn2IcSTu196mX8130_assertion
;
np:hasProvenance
dgn-np:NP470727.RAgPCbJfwRtxHuiwd2sVu-0vqaZUoqOWn2IcSTu196mX8130_provenance
;
np:hasPublicationInfo
dgn-np:NP470727.RAgPCbJfwRtxHuiwd2sVu-0vqaZUoqOWn2IcSTu196mX8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP470727.RAgPCbJfwRtxHuiwd2sVu-0vqaZUoqOWn2IcSTu196mX8130_assertion
a
np:Assertion
.
dgn-np:NP470727.RAgPCbJfwRtxHuiwd2sVu-0vqaZUoqOWn2IcSTu196mX8130_provenance
a
np:Provenance
.
dgn-np:NP470727.RAgPCbJfwRtxHuiwd2sVu-0vqaZUoqOWn2IcSTu196mX8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP470727.RAgPCbJfwRtxHuiwd2sVu-0vqaZUoqOWn2IcSTu196mX8130_assertion
{
miriam-gene:3342
a
ncit:C16612
.
lld:C1853490
a
ncit:C7057
.
dgn-gda:DGN2a3b9b2fa821c19100f3ff72908065ec
sio:SIO_000628
miriam-gene:3342
,
lld:C1853490
;
a
sio:SIO_001122
.
}
dgn-np:NP470727.RAgPCbJfwRtxHuiwd2sVu-0vqaZUoqOWn2IcSTu196mX8130_provenance
{
dgn-np:NP470727.RAgPCbJfwRtxHuiwd2sVu-0vqaZUoqOWn2IcSTu196mX8130_assertion
dcterms:description
"[This study underscores the utility of array CGH for characterising the size and nature of subtelomeric deletions, such as monosomy 22q13, and underlines the considerable variability in deletion size in the 22q13 deletion syndrome regardless of the clinical phenotype.]. 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:15986041
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP470727.RAgPCbJfwRtxHuiwd2sVu-0vqaZUoqOWn2IcSTu196mX8130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:42:17+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}