@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP475910.RAxIoY201dV3H6QzHWBF-2dgjpObQti8DZHAbNQ7fMZNM
> .
@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:NP475910.RAxIoY201dV3H6QzHWBF-2dgjpObQti8DZHAbNQ7fMZNM130_head
{
this:
np:hasAssertion
dgn-np:NP475910.RAxIoY201dV3H6QzHWBF-2dgjpObQti8DZHAbNQ7fMZNM130_assertion
;
np:hasProvenance
dgn-np:NP475910.RAxIoY201dV3H6QzHWBF-2dgjpObQti8DZHAbNQ7fMZNM130_provenance
;
np:hasPublicationInfo
dgn-np:NP475910.RAxIoY201dV3H6QzHWBF-2dgjpObQti8DZHAbNQ7fMZNM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP475910.RAxIoY201dV3H6QzHWBF-2dgjpObQti8DZHAbNQ7fMZNM130_assertion
a
np:Assertion
.
dgn-np:NP475910.RAxIoY201dV3H6QzHWBF-2dgjpObQti8DZHAbNQ7fMZNM130_provenance
a
np:Provenance
.
dgn-np:NP475910.RAxIoY201dV3H6QzHWBF-2dgjpObQti8DZHAbNQ7fMZNM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP475910.RAxIoY201dV3H6QzHWBF-2dgjpObQti8DZHAbNQ7fMZNM130_assertion
{
miriam-gene:3342
a
ncit:C16612
.
lld:C1297882
a
ncit:C7057
.
dgn-gda:DGNafb31595bf5023d5f4034a811c53c827
sio:SIO_000628
miriam-gene:3342
,
lld:C1297882
;
a
sio:SIO_001121
.
}
dgn-np:NP475910.RAxIoY201dV3H6QzHWBF-2dgjpObQti8DZHAbNQ7fMZNM130_provenance
{
dgn-np:NP475910.RAxIoY201dV3H6QzHWBF-2dgjpObQti8DZHAbNQ7fMZNM130_assertion
dcterms:description
"[We utilized whole genomic array comparative genome hybridization (CGH) with 4,000 selected bacterial artificial chromosomes (BACs) to define the chromosomal breakpoints and to delineate the extent of the partial trisomy in more detail.]. 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:19119457
;
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:NP475910.RAxIoY201dV3H6QzHWBF-2dgjpObQti8DZHAbNQ7fMZNM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:45+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" .
}