@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP705635.RAA1gVX6hXhzFbqIZZ4DB_PLu4zSVxoS03xA2mvf3lYZY
> .
@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:NP705635.RAA1gVX6hXhzFbqIZZ4DB_PLu4zSVxoS03xA2mvf3lYZY130_head
{
this:
np:hasAssertion
dgn-np:NP705635.RAA1gVX6hXhzFbqIZZ4DB_PLu4zSVxoS03xA2mvf3lYZY130_assertion
;
np:hasProvenance
dgn-np:NP705635.RAA1gVX6hXhzFbqIZZ4DB_PLu4zSVxoS03xA2mvf3lYZY130_provenance
;
np:hasPublicationInfo
dgn-np:NP705635.RAA1gVX6hXhzFbqIZZ4DB_PLu4zSVxoS03xA2mvf3lYZY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP705635.RAA1gVX6hXhzFbqIZZ4DB_PLu4zSVxoS03xA2mvf3lYZY130_assertion
a
np:Assertion
.
dgn-np:NP705635.RAA1gVX6hXhzFbqIZZ4DB_PLu4zSVxoS03xA2mvf3lYZY130_provenance
a
np:Provenance
.
dgn-np:NP705635.RAA1gVX6hXhzFbqIZZ4DB_PLu4zSVxoS03xA2mvf3lYZY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP705635.RAA1gVX6hXhzFbqIZZ4DB_PLu4zSVxoS03xA2mvf3lYZY130_assertion
{
miriam-gene:3342
a
ncit:C16612
.
lld:C1947901
a
ncit:C7057
.
dgn-gda:DGNec01382ceb4780ecf8e1843f6066b823
sio:SIO_000628
miriam-gene:3342
,
lld:C1947901
;
a
sio:SIO_001121
.
}
dgn-np:NP705635.RAA1gVX6hXhzFbqIZZ4DB_PLu4zSVxoS03xA2mvf3lYZY130_provenance
{
dgn-np:NP705635.RAA1gVX6hXhzFbqIZZ4DB_PLu4zSVxoS03xA2mvf3lYZY130_assertion
dcterms:description
"[We compared the Comparative Genomic Hybridization (CGH) profiles of 20 follicular (FTCs), 12 poorly differentiated (PDTCs) and seven anaplastic thyroid carcinomas (ATCs), in order to identify the chromosomal imbalances potentially associated with cancer progression.]. 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:14735198
;
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:NP705635.RAA1gVX6hXhzFbqIZZ4DB_PLu4zSVxoS03xA2mvf3lYZY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:09+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" .
}