@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP635820.RA4F_1F-_l_tuHQw8uCBAaj4L9qHc2ZNrXBR-NLOyic-s
> .
@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:NP635820.RA4F_1F-_l_tuHQw8uCBAaj4L9qHc2ZNrXBR-NLOyic-s130_head
{
this:
np:hasAssertion
dgn-np:NP635820.RA4F_1F-_l_tuHQw8uCBAaj4L9qHc2ZNrXBR-NLOyic-s130_assertion
;
np:hasProvenance
dgn-np:NP635820.RA4F_1F-_l_tuHQw8uCBAaj4L9qHc2ZNrXBR-NLOyic-s130_provenance
;
np:hasPublicationInfo
dgn-np:NP635820.RA4F_1F-_l_tuHQw8uCBAaj4L9qHc2ZNrXBR-NLOyic-s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP635820.RA4F_1F-_l_tuHQw8uCBAaj4L9qHc2ZNrXBR-NLOyic-s130_assertion
a
np:Assertion
.
dgn-np:NP635820.RA4F_1F-_l_tuHQw8uCBAaj4L9qHc2ZNrXBR-NLOyic-s130_provenance
a
np:Provenance
.
dgn-np:NP635820.RA4F_1F-_l_tuHQw8uCBAaj4L9qHc2ZNrXBR-NLOyic-s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP635820.RA4F_1F-_l_tuHQw8uCBAaj4L9qHc2ZNrXBR-NLOyic-s130_assertion
{
miriam-gene:7253
a
ncit:C16612
.
lld:C1262098
a
ncit:C7057
.
dgn-gda:DGN1c89e713e2c85c2e83a51494a545215b
sio:SIO_000628
miriam-gene:7253
,
lld:C1262098
;
a
sio:SIO_001121
.
}
dgn-np:NP635820.RA4F_1F-_l_tuHQw8uCBAaj4L9qHc2ZNrXBR-NLOyic-s130_provenance
{
dgn-np:NP635820.RA4F_1F-_l_tuHQw8uCBAaj4L9qHc2ZNrXBR-NLOyic-s130_assertion
dcterms:description
"[In order to compare the oncogenic potential of the activated mutant Gs alpha protein and the constitutively activated TSHR, we have transfected FRTL-5 cells with an expression vector bearing either the cDNA of the Gs alpha gene carrying the A201S mutation or the cDNA of the TSH receptor carrying the M453T mutation recently identified in a case of congenital hyperthyroidism.]. 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:9519872
;
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:NP635820.RA4F_1F-_l_tuHQw8uCBAaj4L9qHc2ZNrXBR-NLOyic-s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:23+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" .
}