@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP239203.RA9VVS9w9mVVdxv9JBD2R6f2oFc61_w0jsH_nAWXb--cc
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP239203.RA9VVS9w9mVVdxv9JBD2R6f2oFc61_w0jsH_nAWXb--cc130_head
{
this:
np:hasAssertion
dgn-np:NP239203.RA9VVS9w9mVVdxv9JBD2R6f2oFc61_w0jsH_nAWXb--cc130_assertion
;
np:hasProvenance
dgn-np:NP239203.RA9VVS9w9mVVdxv9JBD2R6f2oFc61_w0jsH_nAWXb--cc130_provenance
;
np:hasPublicationInfo
dgn-np:NP239203.RA9VVS9w9mVVdxv9JBD2R6f2oFc61_w0jsH_nAWXb--cc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP239203.RA9VVS9w9mVVdxv9JBD2R6f2oFc61_w0jsH_nAWXb--cc130_assertion
a
np:Assertion
.
dgn-np:NP239203.RA9VVS9w9mVVdxv9JBD2R6f2oFc61_w0jsH_nAWXb--cc130_provenance
a
np:Provenance
.
dgn-np:NP239203.RA9VVS9w9mVVdxv9JBD2R6f2oFc61_w0jsH_nAWXb--cc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP239203.RA9VVS9w9mVVdxv9JBD2R6f2oFc61_w0jsH_nAWXb--cc130_assertion
{
miriam-gene:292
a
ncit:C16612
.
lld:C2940786
a
ncit:C7057
.
dgn-gda:DGN36f4727ac0ab377358111bb41624612b
sio:SIO_000628
miriam-gene:292
,
lld:C2940786
;
a
sio:SIO_001121
.
}
dgn-np:NP239203.RA9VVS9w9mVVdxv9JBD2R6f2oFc61_w0jsH_nAWXb--cc130_provenance
{
dgn-np:NP239203.RA9VVS9w9mVVdxv9JBD2R6f2oFc61_w0jsH_nAWXb--cc130_assertion
dcterms:description
"[Since similar mutations have been identified in tri-iodothyronine (T3) receptor (TR) beta gene in GRTH and PRTH, and since considerable overlap has been seen in the clinical manifestations in patients with GRTH and PRTH, two subtypes of RTH are now considered to be a continuous spectrum with the same genetic defect.]. 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:8958790
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP239203.RA9VVS9w9mVVdxv9JBD2R6f2oFc61_w0jsH_nAWXb--cc130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:39:56+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}