@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP793355.RA2gGJHZa51VqbhEpVwYKJSnDxiAv7jNfDbcgdAvCbdk0
> .
@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:NP793355.RA2gGJHZa51VqbhEpVwYKJSnDxiAv7jNfDbcgdAvCbdk0130_head
{
this:
np:hasAssertion
dgn-np:NP793355.RA2gGJHZa51VqbhEpVwYKJSnDxiAv7jNfDbcgdAvCbdk0130_assertion
;
np:hasProvenance
dgn-np:NP793355.RA2gGJHZa51VqbhEpVwYKJSnDxiAv7jNfDbcgdAvCbdk0130_provenance
;
np:hasPublicationInfo
dgn-np:NP793355.RA2gGJHZa51VqbhEpVwYKJSnDxiAv7jNfDbcgdAvCbdk0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP793355.RA2gGJHZa51VqbhEpVwYKJSnDxiAv7jNfDbcgdAvCbdk0130_assertion
a
np:Assertion
.
dgn-np:NP793355.RA2gGJHZa51VqbhEpVwYKJSnDxiAv7jNfDbcgdAvCbdk0130_provenance
a
np:Provenance
.
dgn-np:NP793355.RA2gGJHZa51VqbhEpVwYKJSnDxiAv7jNfDbcgdAvCbdk0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP793355.RA2gGJHZa51VqbhEpVwYKJSnDxiAv7jNfDbcgdAvCbdk0130_assertion
{
miriam-gene:8031
a
ncit:C16612
.
lld:C0549473
a
ncit:C7057
.
dgn-gda:DGN6448099a76a89e2231fdc31fb06caf90
sio:SIO_000628
miriam-gene:8031
,
lld:C0549473
;
a
sio:SIO_001121
.
}
dgn-np:NP793355.RA2gGJHZa51VqbhEpVwYKJSnDxiAv7jNfDbcgdAvCbdk0130_provenance
{
dgn-np:NP793355.RA2gGJHZa51VqbhEpVwYKJSnDxiAv7jNfDbcgdAvCbdk0130_assertion
dcterms:description
"[Intrachromosomal rearrangements involving the RET and the adjacent H4 or ELE1 gene are very frequent events in thyroid cancer of children from Belarus after the Chernobyl reactor accident (Klugbauer et al., 1995).]. 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:8806700
;
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:NP793355.RA2gGJHZa51VqbhEpVwYKJSnDxiAv7jNfDbcgdAvCbdk0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:07+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" .
}