@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP756921.RANrGmTdZhWKqFUtBUIjLaGyc2DO_oE3VxJcu5Tlg-OR0
> .
@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:NP756921.RANrGmTdZhWKqFUtBUIjLaGyc2DO_oE3VxJcu5Tlg-OR0130_head
{
this:
np:hasAssertion
dgn-np:NP756921.RANrGmTdZhWKqFUtBUIjLaGyc2DO_oE3VxJcu5Tlg-OR0130_assertion
;
np:hasProvenance
dgn-np:NP756921.RANrGmTdZhWKqFUtBUIjLaGyc2DO_oE3VxJcu5Tlg-OR0130_provenance
;
np:hasPublicationInfo
dgn-np:NP756921.RANrGmTdZhWKqFUtBUIjLaGyc2DO_oE3VxJcu5Tlg-OR0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP756921.RANrGmTdZhWKqFUtBUIjLaGyc2DO_oE3VxJcu5Tlg-OR0130_assertion
a
np:Assertion
.
dgn-np:NP756921.RANrGmTdZhWKqFUtBUIjLaGyc2DO_oE3VxJcu5Tlg-OR0130_provenance
a
np:Provenance
.
dgn-np:NP756921.RANrGmTdZhWKqFUtBUIjLaGyc2DO_oE3VxJcu5Tlg-OR0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP756921.RANrGmTdZhWKqFUtBUIjLaGyc2DO_oE3VxJcu5Tlg-OR0130_assertion
{
miriam-gene:7173
a
ncit:C16612
.
lld:C0549473
a
ncit:C7057
.
dgn-gda:DGNf2622b77e6f00dbcb431d8b62f7fd748
sio:SIO_000628
miriam-gene:7173
,
lld:C0549473
;
a
sio:SIO_001121
.
}
dgn-np:NP756921.RANrGmTdZhWKqFUtBUIjLaGyc2DO_oE3VxJcu5Tlg-OR0130_provenance
{
dgn-np:NP756921.RANrGmTdZhWKqFUtBUIjLaGyc2DO_oE3VxJcu5Tlg-OR0130_assertion
dcterms:description
"[The occurrence of thyroid carcinoma in patients with congenital hypothyroidism (CH) caused by dyshormonogenesis is very rare, and has only been reported in one patient harboring mutations in the thyroid peroxidase (TPO) gene.]. 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:22435912
;
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:NP756921.RANrGmTdZhWKqFUtBUIjLaGyc2DO_oE3VxJcu5Tlg-OR0130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:45:17+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" .
}