@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP254208.RAErgaMKfHLEdmqp2grzDyzUBtHeWk0-rFKJ4bFIHKl-A
> .
@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:NP254208.RAErgaMKfHLEdmqp2grzDyzUBtHeWk0-rFKJ4bFIHKl-A130_head
{
this:
np:hasAssertion
dgn-np:NP254208.RAErgaMKfHLEdmqp2grzDyzUBtHeWk0-rFKJ4bFIHKl-A130_assertion
;
np:hasProvenance
dgn-np:NP254208.RAErgaMKfHLEdmqp2grzDyzUBtHeWk0-rFKJ4bFIHKl-A130_provenance
;
np:hasPublicationInfo
dgn-np:NP254208.RAErgaMKfHLEdmqp2grzDyzUBtHeWk0-rFKJ4bFIHKl-A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP254208.RAErgaMKfHLEdmqp2grzDyzUBtHeWk0-rFKJ4bFIHKl-A130_assertion
a
np:Assertion
.
dgn-np:NP254208.RAErgaMKfHLEdmqp2grzDyzUBtHeWk0-rFKJ4bFIHKl-A130_provenance
a
np:Provenance
.
dgn-np:NP254208.RAErgaMKfHLEdmqp2grzDyzUBtHeWk0-rFKJ4bFIHKl-A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP254208.RAErgaMKfHLEdmqp2grzDyzUBtHeWk0-rFKJ4bFIHKl-A130_assertion
{
miriam-gene:3164
a
ncit:C16612
.
lld:C0040128
a
ncit:C7057
.
dgn-gda:DGN2011a61c017668224ad3a41c19b86238
sio:SIO_000628
miriam-gene:3164
,
lld:C0040128
;
a
sio:SIO_001121
.
}
dgn-np:NP254208.RAErgaMKfHLEdmqp2grzDyzUBtHeWk0-rFKJ4bFIHKl-A130_provenance
{
dgn-np:NP254208.RAErgaMKfHLEdmqp2grzDyzUBtHeWk0-rFKJ4bFIHKl-A130_assertion
dcterms:description
"[It has long been speculated that this defect is likely to be caused by an abnormal thyroid hormone receptor (TR), but this hypothesis could not be directly tested until the isolation of two TR genes, TR alpha and TR beta.]. 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:8165897
;
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:NP254208.RAErgaMKfHLEdmqp2grzDyzUBtHeWk0-rFKJ4bFIHKl-A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:22+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" .
}