@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP760527.RA6RpG-LOwTrHDnT01soAxFJqwCC2M1B3MdmrQLh2bym0
> .
@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:NP760527.RA6RpG-LOwTrHDnT01soAxFJqwCC2M1B3MdmrQLh2bym0130_head
{
this:
np:hasAssertion
dgn-np:NP760527.RA6RpG-LOwTrHDnT01soAxFJqwCC2M1B3MdmrQLh2bym0130_assertion
;
np:hasProvenance
dgn-np:NP760527.RA6RpG-LOwTrHDnT01soAxFJqwCC2M1B3MdmrQLh2bym0130_provenance
;
np:hasPublicationInfo
dgn-np:NP760527.RA6RpG-LOwTrHDnT01soAxFJqwCC2M1B3MdmrQLh2bym0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP760527.RA6RpG-LOwTrHDnT01soAxFJqwCC2M1B3MdmrQLh2bym0130_assertion
a
np:Assertion
.
dgn-np:NP760527.RA6RpG-LOwTrHDnT01soAxFJqwCC2M1B3MdmrQLh2bym0130_provenance
a
np:Provenance
.
dgn-np:NP760527.RA6RpG-LOwTrHDnT01soAxFJqwCC2M1B3MdmrQLh2bym0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP760527.RA6RpG-LOwTrHDnT01soAxFJqwCC2M1B3MdmrQLh2bym0130_assertion
{
miriam-gene:7253
a
ncit:C16612
.
lld:C0018213
a
ncit:C7057
.
dgn-gda:DGN6f6812a15188114218013c194b19d889
sio:SIO_000628
miriam-gene:7253
,
lld:C0018213
;
a
sio:SIO_001122
.
}
dgn-np:NP760527.RA6RpG-LOwTrHDnT01soAxFJqwCC2M1B3MdmrQLh2bym0130_provenance
{
dgn-np:NP760527.RA6RpG-LOwTrHDnT01soAxFJqwCC2M1B3MdmrQLh2bym0130_assertion
dcterms:description
"[These findings indicate that rs12101261 and rs179243 are the possible causal SNPs for GD susceptibility in the TSHR gene and could serve as genetic markers to predict the outcome of pTRAb+ in GD patients.]. 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:24144966
;
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:NP760527.RA6RpG-LOwTrHDnT01soAxFJqwCC2M1B3MdmrQLh2bym0130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:45:19+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" .
}