@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP829815.RABzTiNaGq2bBwZSe7qnH9eknLhoL6ZJnxSADPerjVTsU
> .
@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:NP829815.RABzTiNaGq2bBwZSe7qnH9eknLhoL6ZJnxSADPerjVTsU130_head
{
this:
np:hasAssertion
dgn-np:NP829815.RABzTiNaGq2bBwZSe7qnH9eknLhoL6ZJnxSADPerjVTsU130_assertion
;
np:hasProvenance
dgn-np:NP829815.RABzTiNaGq2bBwZSe7qnH9eknLhoL6ZJnxSADPerjVTsU130_provenance
;
np:hasPublicationInfo
dgn-np:NP829815.RABzTiNaGq2bBwZSe7qnH9eknLhoL6ZJnxSADPerjVTsU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP829815.RABzTiNaGq2bBwZSe7qnH9eknLhoL6ZJnxSADPerjVTsU130_assertion
a
np:Assertion
.
dgn-np:NP829815.RABzTiNaGq2bBwZSe7qnH9eknLhoL6ZJnxSADPerjVTsU130_provenance
a
np:Provenance
.
dgn-np:NP829815.RABzTiNaGq2bBwZSe7qnH9eknLhoL6ZJnxSADPerjVTsU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP829815.RABzTiNaGq2bBwZSe7qnH9eknLhoL6ZJnxSADPerjVTsU130_assertion
{
miriam-gene:3342
a
ncit:C16612
.
lld:C0206717
a
ncit:C7057
.
dgn-gda:DGNa41c38218a299db903ff87b2e7f09423
sio:SIO_000628
miriam-gene:3342
,
lld:C0206717
;
a
sio:SIO_001121
.
}
dgn-np:NP829815.RABzTiNaGq2bBwZSe7qnH9eknLhoL6ZJnxSADPerjVTsU130_provenance
{
dgn-np:NP829815.RABzTiNaGq2bBwZSe7qnH9eknLhoL6ZJnxSADPerjVTsU130_assertion
dcterms:description
"[The CGH analysis of three ENB revealed multiple recurrent aberrations including DNA overrepresentations of chromosomal material of the entire chromosome 19, partial gains of the long arms of chromosomes 8, 15, and 22, and deletions of the entire long arm of chromosome 4.]. 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:12165452
;
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:NP829815.RABzTiNaGq2bBwZSe7qnH9eknLhoL6ZJnxSADPerjVTsU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:28+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" .
}