@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP931295.RAD7AeWeow6aYoQG3o_KrGIRwhJsmm0F9yp7R7fCg8bh4
> .
@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:NP931295.RAD7AeWeow6aYoQG3o_KrGIRwhJsmm0F9yp7R7fCg8bh4130_head
{
this:
np:hasAssertion
dgn-np:NP931295.RAD7AeWeow6aYoQG3o_KrGIRwhJsmm0F9yp7R7fCg8bh4130_assertion
;
np:hasProvenance
dgn-np:NP931295.RAD7AeWeow6aYoQG3o_KrGIRwhJsmm0F9yp7R7fCg8bh4130_provenance
;
np:hasPublicationInfo
dgn-np:NP931295.RAD7AeWeow6aYoQG3o_KrGIRwhJsmm0F9yp7R7fCg8bh4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP931295.RAD7AeWeow6aYoQG3o_KrGIRwhJsmm0F9yp7R7fCg8bh4130_assertion
a
np:Assertion
.
dgn-np:NP931295.RAD7AeWeow6aYoQG3o_KrGIRwhJsmm0F9yp7R7fCg8bh4130_provenance
a
np:Provenance
.
dgn-np:NP931295.RAD7AeWeow6aYoQG3o_KrGIRwhJsmm0F9yp7R7fCg8bh4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP931295.RAD7AeWeow6aYoQG3o_KrGIRwhJsmm0F9yp7R7fCg8bh4130_assertion
{
miriam-gene:6528
a
ncit:C16612
.
lld:C0178468
a
ncit:C7057
.
dgn-gda:DGN089b18ef4e269787d840cf85b14c825b
sio:SIO_000628
miriam-gene:6528
,
lld:C0178468
;
a
sio:SIO_001121
.
}
dgn-np:NP931295.RAD7AeWeow6aYoQG3o_KrGIRwhJsmm0F9yp7R7fCg8bh4130_provenance
{
dgn-np:NP931295.RAD7AeWeow6aYoQG3o_KrGIRwhJsmm0F9yp7R7fCg8bh4130_assertion
dcterms:description
"[The biogenesis and posttranslational modifications of NIS have been examined, a thorough electrophysiological analysis of NIS has been conducted, the cDNA encoding human NIS (hNIS) has been isolated, the genomic organization of hNIS has been elucidated, the regulation of NIS by thyrotropin and I(-) has been analyzed, the regulation of NIS transcription has been studied, spontaneous NIS mutations have been identified as causes of congenital iodide transport defect resulting in hypothyroidism, the roles of NIS in thyroid cancer and thyroid autoimmune disease have been examined, and the expression and regulation of NIS in extrathyroidal tissues have been investigated.]. 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:10893432
;
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:NP931295.RAD7AeWeow6aYoQG3o_KrGIRwhJsmm0F9yp7R7fCg8bh4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:31+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" .
}