@prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP30686.RAg-amB4-mvhtGq4RGW6gsyHGkMnoUnWkWtS_o6lmWQ_8130_head { this: np:hasAssertion dgn-np:NP30686.RAg-amB4-mvhtGq4RGW6gsyHGkMnoUnWkWtS_o6lmWQ_8130_assertion; np:hasProvenance dgn-np:NP30686.RAg-amB4-mvhtGq4RGW6gsyHGkMnoUnWkWtS_o6lmWQ_8130_provenance; np:hasPublicationInfo dgn-np:NP30686.RAg-amB4-mvhtGq4RGW6gsyHGkMnoUnWkWtS_o6lmWQ_8130_publicationInfo; a np:Nanopublication . dgn-np:NP30686.RAg-amB4-mvhtGq4RGW6gsyHGkMnoUnWkWtS_o6lmWQ_8130_assertion a np:Assertion . dgn-np:NP30686.RAg-amB4-mvhtGq4RGW6gsyHGkMnoUnWkWtS_o6lmWQ_8130_provenance a np:Provenance . dgn-np:NP30686.RAg-amB4-mvhtGq4RGW6gsyHGkMnoUnWkWtS_o6lmWQ_8130_publicationInfo a np:PublicationInfo . } dgn-np:NP30686.RAg-amB4-mvhtGq4RGW6gsyHGkMnoUnWkWtS_o6lmWQ_8130_assertion { miriam-gene:6657 a ncit:C16612 . lld:C0007137 a ncit:C7057 . dgn-gda:DGNb251d67ce5f9aac638e46f69480474a3 sio:SIO_000628 miriam-gene:6657, lld:C0007137; a sio:SIO_001121 . } dgn-np:NP30686.RAg-amB4-mvhtGq4RGW6gsyHGkMnoUnWkWtS_o6lmWQ_8130_provenance { dgn-np:NP30686.RAg-amB4-mvhtGq4RGW6gsyHGkMnoUnWkWtS_o6lmWQ_8130_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:NP30686.RAg-amB4-mvhtGq4RGW6gsyHGkMnoUnWkWtS_o6lmWQ_8130_publicationInfo { this: dcterms:created "2014-10-02T12:32:13+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetrdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v2.1.0.0" . dgn-void:disgenetrdf pav:version "v2.1.0" . }