@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP510882.RAgQiFTO1kPi50W5qCqwjoN-nkNfTH1fIWZWTcP3rIJv4
> .
@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:NP510882.RAgQiFTO1kPi50W5qCqwjoN-nkNfTH1fIWZWTcP3rIJv4130_head
{
this:
np:hasAssertion
dgn-np:NP510882.RAgQiFTO1kPi50W5qCqwjoN-nkNfTH1fIWZWTcP3rIJv4130_assertion
;
np:hasProvenance
dgn-np:NP510882.RAgQiFTO1kPi50W5qCqwjoN-nkNfTH1fIWZWTcP3rIJv4130_provenance
;
np:hasPublicationInfo
dgn-np:NP510882.RAgQiFTO1kPi50W5qCqwjoN-nkNfTH1fIWZWTcP3rIJv4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP510882.RAgQiFTO1kPi50W5qCqwjoN-nkNfTH1fIWZWTcP3rIJv4130_assertion
a
np:Assertion
.
dgn-np:NP510882.RAgQiFTO1kPi50W5qCqwjoN-nkNfTH1fIWZWTcP3rIJv4130_provenance
a
np:Provenance
.
dgn-np:NP510882.RAgQiFTO1kPi50W5qCqwjoN-nkNfTH1fIWZWTcP3rIJv4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP510882.RAgQiFTO1kPi50W5qCqwjoN-nkNfTH1fIWZWTcP3rIJv4130_assertion
{
miriam-gene:6657
a
ncit:C16612
.
lld:C0000768
a
ncit:C7057
.
dgn-gda:DGN1971f342213fcc58def45c89a979b91f
sio:SIO_000628
miriam-gene:6657
,
lld:C0000768
;
a
sio:SIO_001121
.
}
dgn-np:NP510882.RAgQiFTO1kPi50W5qCqwjoN-nkNfTH1fIWZWTcP3rIJv4130_provenance
{
dgn-np:NP510882.RAgQiFTO1kPi50W5qCqwjoN-nkNfTH1fIWZWTcP3rIJv4130_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_literature
;
sio:SIO_000772
miriam-pubmed:19801978
;
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:NP510882.RAgQiFTO1kPi50W5qCqwjoN-nkNfTH1fIWZWTcP3rIJv4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:04+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" .
}