@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP935079.RA0kQ0vwuoK2-2DUl0hZwyRlyDTODmoNy_pXbr1ChJHdQ
> .
@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:NP935079.RA0kQ0vwuoK2-2DUl0hZwyRlyDTODmoNy_pXbr1ChJHdQ130_head
{
this:
np:hasAssertion
dgn-np:NP935079.RA0kQ0vwuoK2-2DUl0hZwyRlyDTODmoNy_pXbr1ChJHdQ130_assertion
;
np:hasProvenance
dgn-np:NP935079.RA0kQ0vwuoK2-2DUl0hZwyRlyDTODmoNy_pXbr1ChJHdQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP935079.RA0kQ0vwuoK2-2DUl0hZwyRlyDTODmoNy_pXbr1ChJHdQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP935079.RA0kQ0vwuoK2-2DUl0hZwyRlyDTODmoNy_pXbr1ChJHdQ130_assertion
a
np:Assertion
.
dgn-np:NP935079.RA0kQ0vwuoK2-2DUl0hZwyRlyDTODmoNy_pXbr1ChJHdQ130_provenance
a
np:Provenance
.
dgn-np:NP935079.RA0kQ0vwuoK2-2DUl0hZwyRlyDTODmoNy_pXbr1ChJHdQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP935079.RA0kQ0vwuoK2-2DUl0hZwyRlyDTODmoNy_pXbr1ChJHdQ130_assertion
{
miriam-gene:7200
a
ncit:C16612
.
lld:C0040156
a
ncit:C7057
.
dgn-gda:DGN511caadf2041fb5888cd70b0852c7efe
sio:SIO_000628
miriam-gene:7200
,
lld:C0040156
;
a
sio:SIO_001121
.
}
dgn-np:NP935079.RA0kQ0vwuoK2-2DUl0hZwyRlyDTODmoNy_pXbr1ChJHdQ130_provenance
{
dgn-np:NP935079.RA0kQ0vwuoK2-2DUl0hZwyRlyDTODmoNy_pXbr1ChJHdQ130_assertion
dcterms:description
"[It is suggested that 1) among euthyroid relatives with a family history of Graves' disease, there are many with abnormalities in TRH responsiveness and T3 suppressibility, 2) nonsuppressible subjects are more likely to be TRH hyporesponders and vice versa, 3) hyperthyroidism or hypothyroidism occurs frequently in euthyroid relatives with a family history of Graves' disease, and 4) thyrotoxicosis occurs frequently in TRH-hyporesponders, and hypothyroidism occurs in the others.]. 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:6774999
;
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:NP935079.RA0kQ0vwuoK2-2DUl0hZwyRlyDTODmoNy_pXbr1ChJHdQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:33+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" .
}