@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP918560.RAYMPaWDhE2gSpGGZ5hAYBuY912jw4kB_h_RjV934lI_E
> .
@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:NP918560.RAYMPaWDhE2gSpGGZ5hAYBuY912jw4kB_h_RjV934lI_E130_head
{
this:
np:hasAssertion
dgn-np:NP918560.RAYMPaWDhE2gSpGGZ5hAYBuY912jw4kB_h_RjV934lI_E130_assertion
;
np:hasProvenance
dgn-np:NP918560.RAYMPaWDhE2gSpGGZ5hAYBuY912jw4kB_h_RjV934lI_E130_provenance
;
np:hasPublicationInfo
dgn-np:NP918560.RAYMPaWDhE2gSpGGZ5hAYBuY912jw4kB_h_RjV934lI_E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP918560.RAYMPaWDhE2gSpGGZ5hAYBuY912jw4kB_h_RjV934lI_E130_assertion
a
np:Assertion
.
dgn-np:NP918560.RAYMPaWDhE2gSpGGZ5hAYBuY912jw4kB_h_RjV934lI_E130_provenance
a
np:Provenance
.
dgn-np:NP918560.RAYMPaWDhE2gSpGGZ5hAYBuY912jw4kB_h_RjV934lI_E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP918560.RAYMPaWDhE2gSpGGZ5hAYBuY912jw4kB_h_RjV934lI_E130_assertion
{
miriam-gene:7068
a
ncit:C16612
.
lld:C0018021
a
ncit:C7057
.
dgn-gda:DGNd1720c650e64a26c7c3e23297e8bbe8e
sio:SIO_000628
miriam-gene:7068
,
lld:C0018021
;
a
sio:SIO_001121
.
}
dgn-np:NP918560.RAYMPaWDhE2gSpGGZ5hAYBuY912jw4kB_h_RjV934lI_E130_provenance
{
dgn-np:NP918560.RAYMPaWDhE2gSpGGZ5hAYBuY912jw4kB_h_RjV934lI_E130_assertion
dcterms:description
"[While goiter and thyroid test abnormalities have more often led to the suspicion of thyroid gland dysfunction, short stature, hyperactivity, learning disability and goiter in children or adolescents and recalcitrant goiter in adults, should raise the suspicion of GRTH.]. 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:NP918560.RAYMPaWDhE2gSpGGZ5hAYBuY912jw4kB_h_RjV934lI_E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:23+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" .
}