@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP884958.RAse5XziiEMgD12GR_W9GB0UiQRuTxfeM1lWCgB2lViqo
> .
@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:NP884958.RAse5XziiEMgD12GR_W9GB0UiQRuTxfeM1lWCgB2lViqo130_head
{
this:
np:hasAssertion
dgn-np:NP884958.RAse5XziiEMgD12GR_W9GB0UiQRuTxfeM1lWCgB2lViqo130_assertion
;
np:hasProvenance
dgn-np:NP884958.RAse5XziiEMgD12GR_W9GB0UiQRuTxfeM1lWCgB2lViqo130_provenance
;
np:hasPublicationInfo
dgn-np:NP884958.RAse5XziiEMgD12GR_W9GB0UiQRuTxfeM1lWCgB2lViqo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP884958.RAse5XziiEMgD12GR_W9GB0UiQRuTxfeM1lWCgB2lViqo130_assertion
a
np:Assertion
.
dgn-np:NP884958.RAse5XziiEMgD12GR_W9GB0UiQRuTxfeM1lWCgB2lViqo130_provenance
a
np:Provenance
.
dgn-np:NP884958.RAse5XziiEMgD12GR_W9GB0UiQRuTxfeM1lWCgB2lViqo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP884958.RAse5XziiEMgD12GR_W9GB0UiQRuTxfeM1lWCgB2lViqo130_assertion
{
miriam-gene:7080
a
ncit:C16612
.
lld:C0018021
a
ncit:C7057
.
dgn-gda:DGN978aa3975e542f8e39dbc586193adbca
sio:SIO_000628
miriam-gene:7080
,
lld:C0018021
;
a
sio:SIO_001121
.
}
dgn-np:NP884958.RAse5XziiEMgD12GR_W9GB0UiQRuTxfeM1lWCgB2lViqo130_provenance
{
dgn-np:NP884958.RAse5XziiEMgD12GR_W9GB0UiQRuTxfeM1lWCgB2lViqo130_assertion
dcterms:description
"[A group of 61 patients with CH (22 with agenesis, 18 with ectopy, 1 with hypoplasia, and 20 cases with CH without thyroid enlargement but not further characterized) and 30 normal subjects were examined for the presence of mutations in the gene encoding the thyroid transcription factor 1 (TTF-1).]. 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:9226207
;
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:NP884958.RAse5XziiEMgD12GR_W9GB0UiQRuTxfeM1lWCgB2lViqo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:00+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" .
}