@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP848189.RA0u8pCowFHhdu4H1txHOYDaBnAbkUV6BH3EzMscVXwtc
> .
@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/
> .
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{
this:
np:hasAssertion
dgn-np:NP848189.RA0u8pCowFHhdu4H1txHOYDaBnAbkUV6BH3EzMscVXwtc130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP848189.RA0u8pCowFHhdu4H1txHOYDaBnAbkUV6BH3EzMscVXwtc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP848189.RA0u8pCowFHhdu4H1txHOYDaBnAbkUV6BH3EzMscVXwtc130_assertion
a
np:Assertion
.
dgn-np:NP848189.RA0u8pCowFHhdu4H1txHOYDaBnAbkUV6BH3EzMscVXwtc130_provenance
a
np:Provenance
.
dgn-np:NP848189.RA0u8pCowFHhdu4H1txHOYDaBnAbkUV6BH3EzMscVXwtc130_publicationInfo
a
np:PublicationInfo
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{
miriam-gene:5308
a
ncit:C16612
.
lld:C0032002
a
ncit:C7057
.
dgn-gda:DGN85ee93e4ed920ca860b12a016496791d
sio:SIO_000628
miriam-gene:5308
,
lld:C0032002
;
a
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.
}
dgn-np:NP848189.RA0u8pCowFHhdu4H1txHOYDaBnAbkUV6BH3EzMscVXwtc130_provenance
{
dgn-np:NP848189.RA0u8pCowFHhdu4H1txHOYDaBnAbkUV6BH3EzMscVXwtc130_assertion
dcterms:description
"[In this work, we have investigated the functional properties of three PITX2 mutants reported in Axenfeld-Rieger syndrome patients relative to the regulation of these genes, using reporter genes under the control of human PRL (hPRL), hGH, or POU1F1 promoters transfected in nonpituitary and pituitary cell lines.]. 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:20978111
;
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 .
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dgn-np:NP848189.RA0u8pCowFHhdu4H1txHOYDaBnAbkUV6BH3EzMscVXwtc130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:09+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
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;
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
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"v4.0.0" .
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