@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP430881.RAAoXEK0BfrCpDge2kO40yQVD0-IChm2XMMmM1az9z43k
> .
@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:NP430881.RAAoXEK0BfrCpDge2kO40yQVD0-IChm2XMMmM1az9z43k130_head
{
this:
np:hasAssertion
dgn-np:NP430881.RAAoXEK0BfrCpDge2kO40yQVD0-IChm2XMMmM1az9z43k130_assertion
;
np:hasProvenance
dgn-np:NP430881.RAAoXEK0BfrCpDge2kO40yQVD0-IChm2XMMmM1az9z43k130_provenance
;
np:hasPublicationInfo
dgn-np:NP430881.RAAoXEK0BfrCpDge2kO40yQVD0-IChm2XMMmM1az9z43k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP430881.RAAoXEK0BfrCpDge2kO40yQVD0-IChm2XMMmM1az9z43k130_assertion
a
np:Assertion
.
dgn-np:NP430881.RAAoXEK0BfrCpDge2kO40yQVD0-IChm2XMMmM1az9z43k130_provenance
a
np:Provenance
.
dgn-np:NP430881.RAAoXEK0BfrCpDge2kO40yQVD0-IChm2XMMmM1az9z43k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP430881.RAAoXEK0BfrCpDge2kO40yQVD0-IChm2XMMmM1az9z43k130_assertion
{
miriam-gene:7068
a
ncit:C16612
.
lld:C2940786
a
ncit:C7057
.
dgn-gda:DGNf61d422093ca04c6562ac85a078d3895
sio:SIO_000628
miriam-gene:7068
,
lld:C2940786
;
a
sio:SIO_001121
.
}
dgn-np:NP430881.RAAoXEK0BfrCpDge2kO40yQVD0-IChm2XMMmM1az9z43k130_provenance
{
dgn-np:NP430881.RAAoXEK0BfrCpDge2kO40yQVD0-IChm2XMMmM1az9z43k130_assertion
dcterms:description
"[In almost all cases it is due to different mutations in only one allele of the thyroid hormone receptor beta gene which blocks the action of normal allele thus producing dominantly inherited RTH.]. 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:16444158
;
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:NP430881.RAAoXEK0BfrCpDge2kO40yQVD0-IChm2XMMmM1az9z43k130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:15+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" .
}