@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP869735.RAyRRUfpLjyOBZunPfB1-rEg9pd8OhJP8f0sksEx-fLNU
> .
@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:NP869735.RAyRRUfpLjyOBZunPfB1-rEg9pd8OhJP8f0sksEx-fLNU130_head
{
this:
np:hasAssertion
dgn-np:NP869735.RAyRRUfpLjyOBZunPfB1-rEg9pd8OhJP8f0sksEx-fLNU130_assertion
;
np:hasProvenance
dgn-np:NP869735.RAyRRUfpLjyOBZunPfB1-rEg9pd8OhJP8f0sksEx-fLNU130_provenance
;
np:hasPublicationInfo
dgn-np:NP869735.RAyRRUfpLjyOBZunPfB1-rEg9pd8OhJP8f0sksEx-fLNU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP869735.RAyRRUfpLjyOBZunPfB1-rEg9pd8OhJP8f0sksEx-fLNU130_assertion
a
np:Assertion
.
dgn-np:NP869735.RAyRRUfpLjyOBZunPfB1-rEg9pd8OhJP8f0sksEx-fLNU130_provenance
a
np:Provenance
.
dgn-np:NP869735.RAyRRUfpLjyOBZunPfB1-rEg9pd8OhJP8f0sksEx-fLNU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP869735.RAyRRUfpLjyOBZunPfB1-rEg9pd8OhJP8f0sksEx-fLNU130_assertion
{
miriam-gene:1733
a
ncit:C16612
.
lld:C0027651
a
ncit:C7057
.
dgn-gda:DGN8473675c19a106c9efffc6a827e5bebb
sio:SIO_000628
miriam-gene:1733
,
lld:C0027651
;
a
sio:SIO_001121
.
}
dgn-np:NP869735.RAyRRUfpLjyOBZunPfB1-rEg9pd8OhJP8f0sksEx-fLNU130_provenance
{
dgn-np:NP869735.RAyRRUfpLjyOBZunPfB1-rEg9pd8OhJP8f0sksEx-fLNU130_assertion
dcterms:description
"[Polymorphisms in the DIO1 gene have been associated with changes in serum thyroid hormone levels, whereas decreased D1 activity has been reported in the nonthyroid illness syndrome and in several human neoplasias.]. 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:21415143
;
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:NP869735.RAyRRUfpLjyOBZunPfB1-rEg9pd8OhJP8f0sksEx-fLNU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:52+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" .
}