@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP709194.RAkXi9gk5WmO8qvqLE7YqINF6aBeroWWoBO4_k-a6Wt4Y
> .
@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:NP709194.RAkXi9gk5WmO8qvqLE7YqINF6aBeroWWoBO4_k-a6Wt4Y130_head
{
this:
np:hasAssertion
dgn-np:NP709194.RAkXi9gk5WmO8qvqLE7YqINF6aBeroWWoBO4_k-a6Wt4Y130_assertion
;
np:hasProvenance
dgn-np:NP709194.RAkXi9gk5WmO8qvqLE7YqINF6aBeroWWoBO4_k-a6Wt4Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP709194.RAkXi9gk5WmO8qvqLE7YqINF6aBeroWWoBO4_k-a6Wt4Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP709194.RAkXi9gk5WmO8qvqLE7YqINF6aBeroWWoBO4_k-a6Wt4Y130_assertion
a
np:Assertion
.
dgn-np:NP709194.RAkXi9gk5WmO8qvqLE7YqINF6aBeroWWoBO4_k-a6Wt4Y130_provenance
a
np:Provenance
.
dgn-np:NP709194.RAkXi9gk5WmO8qvqLE7YqINF6aBeroWWoBO4_k-a6Wt4Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP709194.RAkXi9gk5WmO8qvqLE7YqINF6aBeroWWoBO4_k-a6Wt4Y130_assertion
{
miriam-gene:6528
a
ncit:C16612
.
lld:C0342200
a
ncit:C7057
.
dgn-gda:DGNa1c293602f2544aba2e2eb0789590d08
sio:SIO_000628
miriam-gene:6528
,
lld:C0342200
;
a
sio:SIO_001121
.
}
dgn-np:NP709194.RAkXi9gk5WmO8qvqLE7YqINF6aBeroWWoBO4_k-a6Wt4Y130_provenance
{
dgn-np:NP709194.RAkXi9gk5WmO8qvqLE7YqINF6aBeroWWoBO4_k-a6Wt4Y130_assertion
dcterms:description
"[Molecular cloning of the NIS gene in 1996 allowed examination of the molecular basis of congenital hypothyroidism due to iodide transport defect (ITD) many years after the first case was described by Federman et al.]. 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:20153805
;
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:NP709194.RAkXi9gk5WmO8qvqLE7YqINF6aBeroWWoBO4_k-a6Wt4Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:11+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" .
}