@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:NP299271.RA7K0asL8eD4HboXWDgvsHMSX-8YTiVuiJUx1-Dl0veGc130_head { this: np:hasAssertion dgn-np:NP299271.RA7K0asL8eD4HboXWDgvsHMSX-8YTiVuiJUx1-Dl0veGc130_assertion; np:hasProvenance dgn-np:NP299271.RA7K0asL8eD4HboXWDgvsHMSX-8YTiVuiJUx1-Dl0veGc130_provenance; np:hasPublicationInfo dgn-np:NP299271.RA7K0asL8eD4HboXWDgvsHMSX-8YTiVuiJUx1-Dl0veGc130_publicationInfo; a np:Nanopublication . dgn-np:NP299271.RA7K0asL8eD4HboXWDgvsHMSX-8YTiVuiJUx1-Dl0veGc130_assertion a np:Assertion . dgn-np:NP299271.RA7K0asL8eD4HboXWDgvsHMSX-8YTiVuiJUx1-Dl0veGc130_provenance a np:Provenance . dgn-np:NP299271.RA7K0asL8eD4HboXWDgvsHMSX-8YTiVuiJUx1-Dl0veGc130_publicationInfo a np:PublicationInfo . } dgn-np:NP299271.RA7K0asL8eD4HboXWDgvsHMSX-8YTiVuiJUx1-Dl0veGc130_assertion { miriam-gene:4692 a ncit:C16612 . lld:C0153594 a ncit:C7057 . dgn-gda:DGN1df08f1edb0c12255ef17c3958fdacb8 sio:SIO_000628 miriam-gene:4692, lld:C0153594; a sio:SIO_001121 . } dgn-np:NP299271.RA7K0asL8eD4HboXWDgvsHMSX-8YTiVuiJUx1-Dl0veGc130_provenance { dgn-np:NP299271.RA7K0asL8eD4HboXWDgvsHMSX-8YTiVuiJUx1-Dl0veGc130_assertion dcterms:description "[In addition, novel pathways and patterns of associated expression in melanoma cells not reported before emerged, including the following: (a) activation of the NOTCH pathway; (b) increased Twist expression and altered expression of additional transcriptional regulators implicated in embryonic development and epidermal/mesenchymal transition; (c) coordinated activation of cancer/testis antigens; (d) coordinated down-regulation of several immune modulation genes, in particular in the IFN pathways; (e) down-regulation of several genes implicated in membrane trafficking events; and (f) down-regulation of growth suppressors, such as the Prader-Willi gene NECDIN, whose function was confirmed by overexpression of ectopic Flag-necdin.]. 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:15289333; 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:NP299271.RA7K0asL8eD4HboXWDgvsHMSX-8YTiVuiJUx1-Dl0veGc130_publicationInfo { this: dcterms:created "2014-10-02T12:34:50+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" . }