@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP58871.RAjDTNUhrPxH4GRwxi7-DRwF1beNHtw6rZh4N8ocOYHZw
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP58871.RAjDTNUhrPxH4GRwxi7-DRwF1beNHtw6rZh4N8ocOYHZw130_assertion
;
np:hasProvenance
dgn-np:NP58871.RAjDTNUhrPxH4GRwxi7-DRwF1beNHtw6rZh4N8ocOYHZw130_provenance
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np:hasPublicationInfo
dgn-np:NP58871.RAjDTNUhrPxH4GRwxi7-DRwF1beNHtw6rZh4N8ocOYHZw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP58871.RAjDTNUhrPxH4GRwxi7-DRwF1beNHtw6rZh4N8ocOYHZw130_assertion
a
np:Assertion
.
dgn-np:NP58871.RAjDTNUhrPxH4GRwxi7-DRwF1beNHtw6rZh4N8ocOYHZw130_provenance
a
np:Provenance
.
dgn-np:NP58871.RAjDTNUhrPxH4GRwxi7-DRwF1beNHtw6rZh4N8ocOYHZw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP58871.RAjDTNUhrPxH4GRwxi7-DRwF1beNHtw6rZh4N8ocOYHZw130_assertion
{
miriam-gene:7253
a
ncit:C16612
.
lld:C0018213
a
ncit:C7057
.
dgn-gda:DGN82cbe2139d712dda8eabe7f9e5609c9e
sio:SIO_000628
miriam-gene:7253
,
lld:C0018213
;
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.
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dgn-np:NP58871.RAjDTNUhrPxH4GRwxi7-DRwF1beNHtw6rZh4N8ocOYHZw130_provenance
{
dgn-np:NP58871.RAjDTNUhrPxH4GRwxi7-DRwF1beNHtw6rZh4N8ocOYHZw130_assertion
dcterms:description
"[Together with recent identification of disease susceptibility markers in the region of the TSHr gene, these results are supportive of genetic factors existing in this region that may be in linkage disequilibrium with the inheritance of various TSHr polymorphisms.]. 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:12930595
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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 .
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dgn-np:NP58871.RAjDTNUhrPxH4GRwxi7-DRwF1beNHtw6rZh4N8ocOYHZw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:27+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" .
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"v2.1.0" .
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