@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1173644.RAqPCb5MUqUqKGbI2iARpImQcRrISZigVlZDkaX6KoqJk
> .
@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/v4.0.0/void/
> .
dgn-np:NP1173644.RAqPCb5MUqUqKGbI2iARpImQcRrISZigVlZDkaX6KoqJk130_head
{
this:
np:hasAssertion
dgn-np:NP1173644.RAqPCb5MUqUqKGbI2iARpImQcRrISZigVlZDkaX6KoqJk130_assertion
;
np:hasProvenance
dgn-np:NP1173644.RAqPCb5MUqUqKGbI2iARpImQcRrISZigVlZDkaX6KoqJk130_provenance
;
np:hasPublicationInfo
dgn-np:NP1173644.RAqPCb5MUqUqKGbI2iARpImQcRrISZigVlZDkaX6KoqJk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1173644.RAqPCb5MUqUqKGbI2iARpImQcRrISZigVlZDkaX6KoqJk130_assertion
a
np:Assertion
.
dgn-np:NP1173644.RAqPCb5MUqUqKGbI2iARpImQcRrISZigVlZDkaX6KoqJk130_provenance
a
np:Provenance
.
dgn-np:NP1173644.RAqPCb5MUqUqKGbI2iARpImQcRrISZigVlZDkaX6KoqJk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1173644.RAqPCb5MUqUqKGbI2iARpImQcRrISZigVlZDkaX6KoqJk130_assertion
{
miriam-gene:50506
a
ncit:C16612
.
lld:C0018021
a
ncit:C7057
.
dgn-gda:DGN90fa1b14feeac2b4e0015c789d8e35bd
sio:SIO_000628
miriam-gene:50506
,
lld:C0018021
;
a
sio:SIO_001121
.
}
dgn-np:NP1173644.RAqPCb5MUqUqKGbI2iARpImQcRrISZigVlZDkaX6KoqJk130_provenance
{
dgn-np:NP1173644.RAqPCb5MUqUqKGbI2iARpImQcRrISZigVlZDkaX6KoqJk130_assertion
dcterms:description
"[Because the relationships between DUOX2 genotypes and clinical phenotypes are extremely complex, however, further studies are needed to identify more mutations in known genes which are involved in CH and goitre.]. 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:24735383
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1173644.RAqPCb5MUqUqKGbI2iARpImQcRrISZigVlZDkaX6KoqJk130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:50:38+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}