@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP30687.RAEOKedMbNDkP_YjJQQPos7rzyU9xK6cc0f5UPuJypBOc
> .
@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:NP30687.RAEOKedMbNDkP_YjJQQPos7rzyU9xK6cc0f5UPuJypBOc130_head
{
this:
np:hasAssertion
dgn-np:NP30687.RAEOKedMbNDkP_YjJQQPos7rzyU9xK6cc0f5UPuJypBOc130_assertion
;
np:hasProvenance
dgn-np:NP30687.RAEOKedMbNDkP_YjJQQPos7rzyU9xK6cc0f5UPuJypBOc130_provenance
;
np:hasPublicationInfo
dgn-np:NP30687.RAEOKedMbNDkP_YjJQQPos7rzyU9xK6cc0f5UPuJypBOc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP30687.RAEOKedMbNDkP_YjJQQPos7rzyU9xK6cc0f5UPuJypBOc130_assertion
a
np:Assertion
.
dgn-np:NP30687.RAEOKedMbNDkP_YjJQQPos7rzyU9xK6cc0f5UPuJypBOc130_provenance
a
np:Provenance
.
dgn-np:NP30687.RAEOKedMbNDkP_YjJQQPos7rzyU9xK6cc0f5UPuJypBOc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP30687.RAEOKedMbNDkP_YjJQQPos7rzyU9xK6cc0f5UPuJypBOc130_assertion
{
miriam-gene:6657
a
ncit:C16612
.
lld:C0279626
a
ncit:C7057
.
dgn-gda:DGN9899f2c273f26d7c25270b7e388af9cf
sio:SIO_000628
miriam-gene:6657
,
lld:C0279626
;
a
sio:SIO_001121
.
}
dgn-np:NP30687.RAEOKedMbNDkP_YjJQQPos7rzyU9xK6cc0f5UPuJypBOc130_provenance
{
dgn-np:NP30687.RAEOKedMbNDkP_YjJQQPos7rzyU9xK6cc0f5UPuJypBOc130_assertion
dcterms:description
"[Here we show that a peak of genomic amplification on chromosome 3q26.33 found in squamous cell carcinomas (SCCs) of the lung and esophagus contains the transcription factor gene SOX2, which is mutated in hereditary human esophageal malformations, is necessary for normal esophageal squamous development, promotes differentiation and proliferation of basal tracheal cells and cooperates in induction of pluripotent stem cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_curated
;
sio:SIO_000772
miriam-pubmed:19801978
;
prov:wasDerivedFrom
dgn-void:ctd_human-20130708
;
prov:wasGeneratedBy
eco:ECO_0000218
.
dgn-void:ctd_human-20130708
pav:importedOn
"2013-07-24"^^
xsd:date
.
dgn-void:source_evidence_curated
a
eco:ECO_0000205
;
rdfs:comment
"Gene-disease associations manually curated."@en ;
rdfs:label
"DisGeNET evidence - CURATED"@en .
}
dgn-np:NP30687.RAEOKedMbNDkP_YjJQQPos7rzyU9xK6cc0f5UPuJypBOc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:13+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" .
}