@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP532781.RAMzc3FnSr9w4V2Tdr5iVb6cd1JS958FLIKcgOLszkLOw
> .
@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:NP532781.RAMzc3FnSr9w4V2Tdr5iVb6cd1JS958FLIKcgOLszkLOw130_head
{
this:
np:hasAssertion
dgn-np:NP532781.RAMzc3FnSr9w4V2Tdr5iVb6cd1JS958FLIKcgOLszkLOw130_assertion
;
np:hasProvenance
dgn-np:NP532781.RAMzc3FnSr9w4V2Tdr5iVb6cd1JS958FLIKcgOLszkLOw130_provenance
;
np:hasPublicationInfo
dgn-np:NP532781.RAMzc3FnSr9w4V2Tdr5iVb6cd1JS958FLIKcgOLszkLOw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP532781.RAMzc3FnSr9w4V2Tdr5iVb6cd1JS958FLIKcgOLszkLOw130_assertion
a
np:Assertion
.
dgn-np:NP532781.RAMzc3FnSr9w4V2Tdr5iVb6cd1JS958FLIKcgOLszkLOw130_provenance
a
np:Provenance
.
dgn-np:NP532781.RAMzc3FnSr9w4V2Tdr5iVb6cd1JS958FLIKcgOLszkLOw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP532781.RAMzc3FnSr9w4V2Tdr5iVb6cd1JS958FLIKcgOLszkLOw130_assertion
{
miriam-gene:472
a
ncit:C16612
.
lld:C0206682
a
ncit:C7057
.
dgn-gda:DGN450a8f83e6305b1820445a8b4066bd4a
sio:SIO_000628
miriam-gene:472
,
lld:C0206682
;
a
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.
}
dgn-np:NP532781.RAMzc3FnSr9w4V2Tdr5iVb6cd1JS958FLIKcgOLszkLOw130_provenance
{
dgn-np:NP532781.RAMzc3FnSr9w4V2Tdr5iVb6cd1JS958FLIKcgOLszkLOw130_assertion
dcterms:description
"[These results unveil the chromosomal regions where genes of interest in thyroid anaplastic transformation are to be located, and demonstrate that different gene dosage copy sequence imbalances are associated to the 'direct' pathway of transformation of follicular into anaplastic cancers and to the progressive FTC --> PDTC --> ATC pathway.]. 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 .
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dgn-np:NP532781.RAMzc3FnSr9w4V2Tdr5iVb6cd1JS958FLIKcgOLszkLOw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:21+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
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pav:authoredBy
<
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> , <
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> , <
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" .
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