@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP575652.RAdCMX3V3x07JjxDlDukKhlj6tL0sKFJXhtdem9Pt1j2M
> .
@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:NP575652.RAdCMX3V3x07JjxDlDukKhlj6tL0sKFJXhtdem9Pt1j2M130_head
{
this:
np:hasAssertion
dgn-np:NP575652.RAdCMX3V3x07JjxDlDukKhlj6tL0sKFJXhtdem9Pt1j2M130_assertion
;
np:hasProvenance
dgn-np:NP575652.RAdCMX3V3x07JjxDlDukKhlj6tL0sKFJXhtdem9Pt1j2M130_provenance
;
np:hasPublicationInfo
dgn-np:NP575652.RAdCMX3V3x07JjxDlDukKhlj6tL0sKFJXhtdem9Pt1j2M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP575652.RAdCMX3V3x07JjxDlDukKhlj6tL0sKFJXhtdem9Pt1j2M130_assertion
a
np:Assertion
.
dgn-np:NP575652.RAdCMX3V3x07JjxDlDukKhlj6tL0sKFJXhtdem9Pt1j2M130_provenance
a
np:Provenance
.
dgn-np:NP575652.RAdCMX3V3x07JjxDlDukKhlj6tL0sKFJXhtdem9Pt1j2M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP575652.RAdCMX3V3x07JjxDlDukKhlj6tL0sKFJXhtdem9Pt1j2M130_assertion
{
miriam-gene:7253
a
ncit:C16612
.
lld:C0302840
a
ncit:C7057
.
dgn-gda:DGN250502aae90b2300090dc09a3408d50c
sio:SIO_000628
miriam-gene:7253
,
lld:C0302840
;
a
sio:SIO_001121
.
}
dgn-np:NP575652.RAdCMX3V3x07JjxDlDukKhlj6tL0sKFJXhtdem9Pt1j2M130_provenance
{
dgn-np:NP575652.RAdCMX3V3x07JjxDlDukKhlj6tL0sKFJXhtdem9Pt1j2M130_assertion
dcterms:description
"[The presence of activating mutations has been demonstrated in the TSH-R gene as well as in the Gs alpha protein gene in thyroid toxic adenoma resulting in the constitutive activation of the cAMP pathway and it has been hypothesised that these genetic alterations may play a causative role in the disease.]. 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:10385711
;
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:NP575652.RAdCMX3V3x07JjxDlDukKhlj6tL0sKFJXhtdem9Pt1j2M130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:47+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" .
}