@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP662355.RAhEWVC4EHix1T1_0TkfCEQ19SPKSC28eTjjvqoY4y8Wc
> .
@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:NP662355.RAhEWVC4EHix1T1_0TkfCEQ19SPKSC28eTjjvqoY4y8Wc130_head
{
this:
np:hasAssertion
dgn-np:NP662355.RAhEWVC4EHix1T1_0TkfCEQ19SPKSC28eTjjvqoY4y8Wc130_assertion
;
np:hasProvenance
dgn-np:NP662355.RAhEWVC4EHix1T1_0TkfCEQ19SPKSC28eTjjvqoY4y8Wc130_provenance
;
np:hasPublicationInfo
dgn-np:NP662355.RAhEWVC4EHix1T1_0TkfCEQ19SPKSC28eTjjvqoY4y8Wc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP662355.RAhEWVC4EHix1T1_0TkfCEQ19SPKSC28eTjjvqoY4y8Wc130_assertion
a
np:Assertion
.
dgn-np:NP662355.RAhEWVC4EHix1T1_0TkfCEQ19SPKSC28eTjjvqoY4y8Wc130_provenance
a
np:Provenance
.
dgn-np:NP662355.RAhEWVC4EHix1T1_0TkfCEQ19SPKSC28eTjjvqoY4y8Wc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP662355.RAhEWVC4EHix1T1_0TkfCEQ19SPKSC28eTjjvqoY4y8Wc130_assertion
{
miriam-gene:7038
a
ncit:C16612
.
lld:C0020550
a
ncit:C7057
.
dgn-gda:DGN8badd739d901542bf2e85856366a19f8
sio:SIO_000628
miriam-gene:7038
,
lld:C0020550
;
a
sio:SIO_001121
.
}
dgn-np:NP662355.RAhEWVC4EHix1T1_0TkfCEQ19SPKSC28eTjjvqoY4y8Wc130_provenance
{
dgn-np:NP662355.RAhEWVC4EHix1T1_0TkfCEQ19SPKSC28eTjjvqoY4y8Wc130_assertion
dcterms:description
"[Because of the diffuse (99 m)Tc uptake and the negative TPO, TSHR, and thyroglobulin antibodies, genetic analysis of her TSHR gene was performed, in spite of her negative family history for hyperthyroidism.]. 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:22763653
;
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:NP662355.RAhEWVC4EHix1T1_0TkfCEQ19SPKSC28eTjjvqoY4y8Wc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:40+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" .
}