@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP250366.RAidqKFUam7a97vlXgfpBdEKZLIL1tZouNsVUI5IiOO-w
> .
@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:NP250366.RAidqKFUam7a97vlXgfpBdEKZLIL1tZouNsVUI5IiOO-w130_head
{
this:
np:hasAssertion
dgn-np:NP250366.RAidqKFUam7a97vlXgfpBdEKZLIL1tZouNsVUI5IiOO-w130_assertion
;
np:hasProvenance
dgn-np:NP250366.RAidqKFUam7a97vlXgfpBdEKZLIL1tZouNsVUI5IiOO-w130_provenance
;
np:hasPublicationInfo
dgn-np:NP250366.RAidqKFUam7a97vlXgfpBdEKZLIL1tZouNsVUI5IiOO-w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP250366.RAidqKFUam7a97vlXgfpBdEKZLIL1tZouNsVUI5IiOO-w130_assertion
a
np:Assertion
.
dgn-np:NP250366.RAidqKFUam7a97vlXgfpBdEKZLIL1tZouNsVUI5IiOO-w130_provenance
a
np:Provenance
.
dgn-np:NP250366.RAidqKFUam7a97vlXgfpBdEKZLIL1tZouNsVUI5IiOO-w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP250366.RAidqKFUam7a97vlXgfpBdEKZLIL1tZouNsVUI5IiOO-w130_assertion
{
miriam-gene:3342
a
ncit:C16612
.
lld:C1297882
a
ncit:C7057
.
dgn-gda:DGN8c9c0e7e87605636292ba6c77922cfa9
sio:SIO_000628
miriam-gene:3342
,
lld:C1297882
;
a
sio:SIO_001121
.
}
dgn-np:NP250366.RAidqKFUam7a97vlXgfpBdEKZLIL1tZouNsVUI5IiOO-w130_provenance
{
dgn-np:NP250366.RAidqKFUam7a97vlXgfpBdEKZLIL1tZouNsVUI5IiOO-w130_assertion
dcterms:description
"[Cytogenetic findings in our tumor after comparative genomic hybridization (CGH) showed full trisomies of chromosomes 20 and 22q, partial trisomies for the distal part of 11q and 1p, and an approximately full monosomy of chromosome 4 (4qter-4p15).]. 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:12149722
;
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:NP250366.RAidqKFUam7a97vlXgfpBdEKZLIL1tZouNsVUI5IiOO-w130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:20+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" .
}