@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP196304.RAlcEn5NkF1rzim1FK2vKC4qVa_7dQpyQpAjL3jcC4hcc
> .
@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:NP196304.RAlcEn5NkF1rzim1FK2vKC4qVa_7dQpyQpAjL3jcC4hcc130_head
{
this:
np:hasAssertion
dgn-np:NP196304.RAlcEn5NkF1rzim1FK2vKC4qVa_7dQpyQpAjL3jcC4hcc130_assertion
;
np:hasProvenance
dgn-np:NP196304.RAlcEn5NkF1rzim1FK2vKC4qVa_7dQpyQpAjL3jcC4hcc130_provenance
;
np:hasPublicationInfo
dgn-np:NP196304.RAlcEn5NkF1rzim1FK2vKC4qVa_7dQpyQpAjL3jcC4hcc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP196304.RAlcEn5NkF1rzim1FK2vKC4qVa_7dQpyQpAjL3jcC4hcc130_assertion
a
np:Assertion
.
dgn-np:NP196304.RAlcEn5NkF1rzim1FK2vKC4qVa_7dQpyQpAjL3jcC4hcc130_provenance
a
np:Provenance
.
dgn-np:NP196304.RAlcEn5NkF1rzim1FK2vKC4qVa_7dQpyQpAjL3jcC4hcc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP196304.RAlcEn5NkF1rzim1FK2vKC4qVa_7dQpyQpAjL3jcC4hcc130_assertion
{
miriam-gene:7253
a
ncit:C16612
.
lld:C0342208
a
ncit:C7057
.
dgn-gda:DGNc799b69053596dec2a1ceda7f0d29a86
sio:SIO_000628
miriam-gene:7253
,
lld:C0342208
;
a
sio:SIO_001121
.
}
dgn-np:NP196304.RAlcEn5NkF1rzim1FK2vKC4qVa_7dQpyQpAjL3jcC4hcc130_provenance
{
dgn-np:NP196304.RAlcEn5NkF1rzim1FK2vKC4qVa_7dQpyQpAjL3jcC4hcc130_assertion
dcterms:description
"[In conclusion, our findings show for the first time that gain-of-function TSHr mutations are not only present in hyperfunctioning thyroid nodules with the histological features of the true thyroid adenomas, but also in hyperfunctioning hyperplastic nodules contained in the same multinodular goiter.]. 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:9709907
;
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:NP196304.RAlcEn5NkF1rzim1FK2vKC4qVa_7dQpyQpAjL3jcC4hcc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:48+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" .
}